Canonical Allele Identifier: CA2729048594

Linked Data

dbSNP Id: rs2138646317

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23417497_23417500del , CM000676.2:g.23417497_23417500del GRCh38
NC_000014.8:g.23886706_23886709del , CM000676.1:g.23886706_23886709del GRCh37
NC_000014.7:g.22956546_22956549del NCBI36
NG_007884.1:g.23162_23165del , LRG_384:g.23162_23165del

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4353+3_4353+6del (MYH7) MANE Select ENSP00000347507.3:n.4353+3_4353+6del
ENST00000355349.3:c.4353+3_4353+6del (MYH7) ENSP00000347507.3:n.4353+3_4353+6del
NM_000257.3:c.4353+3_4353+6del (MYH7) NP_000248.2:n.4353+3_4353+6del
NR_126491.1:n.814-36_814-33del (MHRT)
XM_017021340.1:c.4353+3_4353+6del (MYH7) XP_016876829.1:n.4353+3_4353+6del
NM_000257.4:c.4353+3_4353+6del (MYH7) MANE Select NP_000248.2:n.4353+3_4353+6del