Canonical Allele Identifier: CA384901054

Gene: ACVRL1

Linked Data

• ClinVar Variation Id: 1766394
• ClinVar RCV Id: RCV002371435
• MyVariant Identifiers: chr12:g.52309162G>A (hg19) ; chr12:g.51915378G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51915378G>A , CM000674.2:g.51915378G>A	GRCh38
NC_000012.11:g.52309162G>A , CM000674.1:g.52309162G>A	GRCh37
NC_000012.10:g.50595429G>A	NCBI36
NG_009549.1:g.12961G>A , LRG_543:g.12961G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000547400.6:c.656G>A	ENSP00000446724.2:p.Gly219Asp
ENST00000551576.6:c.926G>A	ENSP00000455848.2:p.Gly309Asp
ENST00000552678.2:c.926G>A	ENSP00000457394.2:p.Gly309Asp
ENST00000388922.9:c.926G>A MANE Select	ENSP00000373574.4:p.Gly309Asp
ENST00000388922.8:c.926G>A	ENSP00000373574.4:p.Gly309Asp
ENST00000419526.6:c.404G>A	ENSP00000392492.2:p.Gly135Asp
ENST00000550683.5:c.968G>A	ENSP00000447884.1:p.Gly323Asp
NM_000020.2:c.926G>A , LRG_543t1:c.926G>A	NP_000011.2:p.Gly309Asp
NM_001077401.1:c.926G>A	NP_001070869.1:p.Gly309Asp
XM_005269235.2:c.926G>A	XP_005269292.1:p.Gly309Asp
XM_011539008.1:c.656G>A	XP_011537310.1:p.Gly219Asp
XM_024449279.1:c.137G>A	XP_024305047.1:p.Gly46Asp
NM_000020.3:c.926G>A MANE Select	NP_000011.2:p.Gly309Asp
NM_001077401.2:c.926G>A	NP_001070869.1:p.Gly309Asp