Canonical Allele Identifier: CA384897359
Gene: ACVRL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.51913099G>T , CM000674.2:g.51913099G>T GRCh38
NC_000012.11:g.52306883G>T , CM000674.1:g.52306883G>T GRCh37
NC_000012.10:g.50593150G>T NCBI36
NG_009549.1:g.10682G>T , LRG_543:g.10682G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000547400.6:c.104G>T ENSP00000446724.2:p.Gly35Val
ENST00000551576.6:c.62G>T ENSP00000455848.2:p.Gly21Val
ENST00000552678.2:c.62G>T ENSP00000457394.2:p.Gly21Val
ENST00000388922.9:c.62G>T MANE Select ENSP00000373574.4:p.Gly21Val
ENST00000388922.8:c.62G>T ENSP00000373574.4:p.Gly21Val
ENST00000419526.6:c.103+564G>T ENSP00000392492.2:n.103+564G>T
ENST00000547400.5:c.104G>T ENSP00000446724.1:p.Gly35Val
ENST00000550683.5:c.104G>T ENSP00000447884.1:p.Gly35Val
ENST00000551576.5:c.62G>T ENSP00000455848.1:p.Gly21Val
NM_000020.2:c.62G>T , LRG_543t1:c.62G>T NP_000011.2:p.Gly21Val
NM_001077401.1:c.62G>T NP_001070869.1:p.Gly21Val
XM_005269235.2:c.62G>T XP_005269292.1:p.Gly21Val
XM_011539008.1:c.104G>T XP_011537310.1:p.Gly35Val
NM_000020.3:c.62G>T MANE Select NP_000011.2:p.Gly21Val
NM_001077401.2:c.62G>T NP_001070869.1:p.Gly21Val