Canonical Allele Identifier: CA6572824

Gene: ACVRL1

Linked Data

• dbSNP Id: rs267606633
• ExAC: 12:52306966 G / A
• gnomAD v2: 12-52306966-G-A
• gnomAD v3: 12-51913182-G-A
• gnomAD v4: 12-51913182-G-A
• MyVariant Identifiers: chr12:g.52306966G>A (hg19) ; chr12:g.51913182G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51913182G>A , CM000674.2:g.51913182G>A	GRCh38
NC_000012.11:g.52306966G>A , CM000674.1:g.52306966G>A	GRCh37
NC_000012.10:g.50593233G>A	NCBI36
NG_009549.1:g.10765G>A , LRG_543:g.10765G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000547400.6:c.187G>A	ENSP00000446724.2:p.Ala63Thr
ENST00000551576.6:c.145G>A	ENSP00000455848.2:p.Ala49Thr
ENST00000552678.2:c.145G>A	ENSP00000457394.2:p.Ala49Thr
ENST00000388922.9:c.145G>A MANE Select	ENSP00000373574.4:p.Ala49Thr
ENST00000388922.8:c.145G>A	ENSP00000373574.4:p.Ala49Thr
ENST00000419526.6:c.103+647G>A	ENSP00000392492.2:n.103+647G>A
ENST00000547400.5:c.187G>A	ENSP00000446724.1:p.Ala63Thr
ENST00000550683.5:c.187G>A	ENSP00000447884.1:p.Ala63Thr
ENST00000551576.5:c.145G>A	ENSP00000455848.1:p.Ala49Thr
NM_000020.2:c.145G>A , LRG_543t1:c.145G>A	NP_000011.2:p.Ala49Thr
NM_001077401.1:c.145G>A	NP_001070869.1:p.Ala49Thr
XM_005269235.2:c.145G>A	XP_005269292.1:p.Ala49Thr
XM_011539008.1:c.187G>A	XP_011537310.1:p.Ala63Thr
NM_000020.3:c.145G>A MANE Select	NP_000011.2:p.Ala49Thr
NM_001077401.2:c.145G>A	NP_001070869.1:p.Ala49Thr