Canonical Allele Identifier: CA384901809

Gene: ACVRL1

Linked Data

• ClinVar Variation Id: 2735872
• ClinVar RCV Id: RCV003508992
• MyVariant Identifiers: chr12:g.52309275G>C (hg19) ; chr12:g.51915491G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51915491G>C , CM000674.2:g.51915491G>C	GRCh38
NC_000012.11:g.52309275G>C , CM000674.1:g.52309275G>C	GRCh37
NC_000012.10:g.50595542G>C	NCBI36
NG_009549.1:g.13074G>C , LRG_543:g.13074G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547400.6:c.769G>C	ENSP00000446724.2:p.Ala257Pro
ENST00000551576.6:c.1039G>C	ENSP00000455848.2:p.Ala347Pro
ENST00000552678.2:c.1039G>C	ENSP00000457394.2:p.Ala347Pro
ENST00000388922.9:c.1039G>C MANE Select	ENSP00000373574.4:p.Ala347Pro
ENST00000388922.8:c.1039G>C	ENSP00000373574.4:p.Ala347Pro
ENST00000419526.6:c.517G>C	ENSP00000392492.2:p.Ala173Pro
ENST00000550683.5:c.1081G>C	ENSP00000447884.1:p.Ala361Pro
ENST00000552678.1:c.44G>C
NM_000020.2:c.1039G>C , LRG_543t1:c.1039G>C	NP_000011.2:p.Ala347Pro
NM_001077401.1:c.1039G>C	NP_001070869.1:p.Ala347Pro
XM_005269235.2:c.1039G>C	XP_005269292.1:p.Ala347Pro
XM_011539008.1:c.769G>C	XP_011537310.1:p.Ala257Pro
XM_024449279.1:c.250G>C	XP_024305047.1:p.Ala84Pro
NM_000020.3:c.1039G>C MANE Select	NP_000011.2:p.Ala347Pro
NM_001077401.2:c.1039G>C	NP_001070869.1:p.Ala347Pro