Canonical Allele Identifier: CA2573953597
Gene: SERPINC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909987A>G , CM000663.2:g.173909987A>G GRCh38
NC_000001.10:g.173879125A>G , CM000663.1:g.173879125A>G GRCh37
NC_000001.9:g.172145748A>G NCBI36
NG_012462.1:g.12392T>C , LRG_577:g.12392T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.763-45T>C MANE Select ENSP00000356671.3:n.763-45T>C
ENST00000367698.3:c.763-45T>C ENSP00000356671.3:n.763-45T>C
ENST00000487183.1:n.414-45T>C
ENST00000617423.4:c.559+1877T>C ENSP00000478688.1:n.559+1877T>C
NM_000488.3:c.763-45T>C , LRG_577t1:c.763-45T>C NP_000479.1:n.763-45T>C
XM_005245198.2:c.619-45T>C XP_005245255.1:n.619-45T>C
NM_001365052.1:c.619-45T>C NP_001351981.1:n.619-45T>C
NM_000488.4:c.763-45T>C MANE Select NP_000479.1:n.763-45T>C
NM_001365052.2:c.619-45T>C NP_001351981.1:n.619-45T>C
NM_001386302.1:c.886-45T>C NP_001373231.1:n.886-45T>C
NM_001386303.1:c.844-45T>C NP_001373232.1:n.844-45T>C
NM_001386304.1:c.742-45T>C NP_001373233.1:n.742-45T>C
NM_001386305.1:c.763-102T>C NP_001373234.1:n.763-102T>C
NM_001386306.1:c.547-45T>C NP_001373235.1:n.547-45T>C