Canonical Allele Identifier: CA384901058

Gene: ACVRL1

Linked Data

• ClinVar Variation Id: 1766395
• ClinVar RCV Id: RCV002371436
• COSMIC: COSM6250606 ; COSM6250607
• MyVariant Identifiers: chr12:g.52309162G>T (hg19) ; chr12:g.51915378G>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000547400.6:c.656G>T	ENSP00000446724.2:p.Gly219Val
ENST00000551576.6:c.926G>T	ENSP00000455848.2:p.Gly309Val
ENST00000552678.2:c.926G>T	ENSP00000457394.2:p.Gly309Val
ENST00000388922.9:c.926G>T MANE Select	ENSP00000373574.4:p.Gly309Val
ENST00000388922.8:c.926G>T	ENSP00000373574.4:p.Gly309Val
ENST00000419526.6:c.404G>T	ENSP00000392492.2:p.Gly135Val
ENST00000550683.5:c.968G>T	ENSP00000447884.1:p.Gly323Val
NM_000020.2:c.926G>T , LRG_543t1:c.926G>T	NP_000011.2:p.Gly309Val
NM_001077401.1:c.926G>T	NP_001070869.1:p.Gly309Val
XM_005269235.2:c.926G>T	XP_005269292.1:p.Gly309Val
XM_011539008.1:c.656G>T	XP_011537310.1:p.Gly219Val
XM_024449279.1:c.137G>T	XP_024305047.1:p.Gly46Val
NM_000020.3:c.926G>T MANE Select	NP_000011.2:p.Gly309Val
NM_001077401.2:c.926G>T	NP_001070869.1:p.Gly309Val