Canonical Allele Identifier: CA343774752
Gene: SERPINC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909910G>T , CM000663.2:g.173909910G>T GRCh38
NC_000001.10:g.173879048G>T , CM000663.1:g.173879048G>T GRCh37
NC_000001.9:g.172145671G>T NCBI36
NG_012462.1:g.12469C>A , LRG_577:g.12469C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.795C>A MANE Select ENSP00000356671.3:p.Asn265Lys
ENST00000367698.3:c.795C>A ENSP00000356671.3:p.Asn265Lys
ENST00000487183.1:n.446C>A
ENST00000617423.4:c.559+1954C>A ENSP00000478688.1:n.559+1954C>A
NM_000488.3:c.795C>A , LRG_577t1:c.795C>A NP_000479.1:p.Asn265Lys
XM_005245198.2:c.651C>A XP_005245255.1:p.Asn217Lys
NM_001365052.1:c.651C>A NP_001351981.1:p.Asn217Lys
NM_000488.4:c.795C>A MANE Select NP_000479.1:p.Asn265Lys
NM_001365052.2:c.651C>A NP_001351981.1:p.Asn217Lys
NM_001386302.1:c.918C>A NP_001373231.1:p.Asn306Lys
NM_001386303.1:c.876C>A NP_001373232.1:p.Asn292Lys
NM_001386304.1:c.774C>A NP_001373233.1:p.Asn258Lys
NM_001386305.1:c.763-25C>A NP_001373234.1:n.763-25C>A
NM_001386306.1:c.579C>A NP_001373235.1:p.Asn193Lys