Canonical Allele Identifier: CA384898726

Gene: ACVRL1

Linked Data

• MyVariant Identifiers: chr12:g.52307435G>A (hg19) ; chr12:g.51913651G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51913651G>A , CM000674.2:g.51913651G>A	GRCh38
NC_000012.11:g.52307435G>A , CM000674.1:g.52307435G>A	GRCh37
NC_000012.10:g.50593702G>A	NCBI36
NG_009549.1:g.11234G>A , LRG_543:g.11234G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547400.6:c.355+301G>A	ENSP00000446724.2:n.355+301G>A
ENST00000551576.6:c.406G>A	ENSP00000455848.2:p.Gly136Ser
ENST00000552678.2:c.406G>A	ENSP00000457394.2:p.Gly136Ser
ENST00000388922.9:c.406G>A MANE Select	ENSP00000373574.4:p.Gly136Ser
ENST00000388922.8:c.406G>A	ENSP00000373574.4:p.Gly136Ser
ENST00000419526.6:c.104-788G>A	ENSP00000392492.2:n.104-788G>A
ENST00000547400.5:c.355+301G>A	ENSP00000446724.1:n.355+301G>A
ENST00000550683.5:c.448G>A	ENSP00000447884.1:p.Gly150Ser
NM_000020.2:c.406G>A , LRG_543t1:c.406G>A	NP_000011.2:p.Gly136Ser
NM_001077401.1:c.406G>A	NP_001070869.1:p.Gly136Ser
XM_005269235.2:c.406G>A	XP_005269292.1:p.Gly136Ser
XM_011539008.1:c.355+301G>A	XP_011537310.1:n.355+301G>A
XM_024449279.1:c.-284G>A	XP_024305047.1:n.-284G>A
NM_000020.3:c.406G>A MANE Select	NP_000011.2:p.Gly136Ser
NM_001077401.2:c.406G>A	NP_001070869.1:p.Gly136Ser