Canonical Allele Identifier: CA384905278

Gene: ACVRL1

Linked Data

• MyVariant Identifiers: chr12:g.52314553G>A (hg19) ; chr12:g.51920769G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51920769G>A , CM000674.2:g.51920769G>A	GRCh38
NC_000012.11:g.52314553G>A , CM000674.1:g.52314553G>A	GRCh37
NC_000012.10:g.50600820G>A	NCBI36
NG_009549.1:g.18352G>A , LRG_543:g.18352G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000547400.6:c.1118G>A	ENSP00000446724.2:p.Gly373Asp
ENST00000551576.6:c.1388G>A	ENSP00000455848.2:p.Gly463Asp
ENST00000388922.9:c.1388G>A MANE Select	ENSP00000373574.4:p.Gly463Asp
ENST00000388922.8:c.1388G>A	ENSP00000373574.4:p.Gly463Asp
ENST00000419526.6:c.866G>A	ENSP00000392492.2:p.Gly289Asp
ENST00000550683.5:c.1430G>A	ENSP00000447884.1:p.Gly477Asp
NM_000020.2:c.1388G>A , LRG_543t1:c.1388G>A	NP_000011.2:p.Gly463Asp
NM_001077401.1:c.1388G>A	NP_001070869.1:p.Gly463Asp
XM_005269235.2:c.1388G>A	XP_005269292.1:p.Gly463Asp
XM_011539008.1:c.1118G>A	XP_011537310.1:p.Gly373Asp
XM_024449279.1:c.599G>A	XP_024305047.1:p.Gly200Asp
NM_000020.3:c.1388G>A MANE Select	NP_000011.2:p.Gly463Asp
NM_001077401.2:c.1388G>A	NP_001070869.1:p.Gly463Asp