Canonical Allele Identifier: CA384900285

Gene: ACVRL1

Linked Data

• dbSNP Id: rs1940801382
• gnomAD v4: 12-51915225-G-C
• MyVariant Identifiers: chr12:g.52309009G>C (hg19) ; chr12:g.51915225G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51915225G>C , CM000674.2:g.51915225G>C	GRCh38
NC_000012.11:g.52309009G>C , CM000674.1:g.52309009G>C	GRCh37
NC_000012.10:g.50595276G>C	NCBI36
NG_009549.1:g.12808G>C , LRG_543:g.12808G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000547400.6:c.503G>C	ENSP00000446724.2:p.Gly168Ala
ENST00000551576.6:c.773G>C	ENSP00000455848.2:p.Gly258Ala
ENST00000552678.2:c.773G>C	ENSP00000457394.2:p.Gly258Ala
ENST00000388922.9:c.773G>C MANE Select	ENSP00000373574.4:p.Gly258Ala
ENST00000388922.8:c.773G>C	ENSP00000373574.4:p.Gly258Ala
ENST00000419526.6:c.251G>C	ENSP00000392492.2:p.Gly84Ala
ENST00000550683.5:c.815G>C	ENSP00000447884.1:p.Gly272Ala
NM_000020.2:c.773G>C , LRG_543t1:c.773G>C	NP_000011.2:p.Gly258Ala
NM_001077401.1:c.773G>C	NP_001070869.1:p.Gly258Ala
XM_005269235.2:c.773G>C	XP_005269292.1:p.Gly258Ala
XM_011539008.1:c.503G>C	XP_011537310.1:p.Gly168Ala
XM_024449279.1:c.-17G>C	XP_024305047.1:n.-17G>C
NM_000020.3:c.773G>C MANE Select	NP_000011.2:p.Gly258Ala
NM_001077401.2:c.773G>C	NP_001070869.1:p.Gly258Ala