Canonical Allele Identifier: CA480063233

Gene: ACVRL1

Linked Data

• ClinVar Variation Id: 2698839
• ClinVar RCV Id: RCV003510471
• MyVariant Identifiers: chr12:g.52309169G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51915385G>C , CM000674.2:g.51915385G>C	GRCh38
NC_000012.11:g.52309169G>C , CM000674.1:g.52309169G>C	GRCh37
NC_000012.10:g.50595436G>C	NCBI36
NG_009549.1:g.12968G>C , LRG_543:g.12968G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000547400.6:c.663G>C	ENSP00000446724.2:p.Ala221=
ENST00000551576.6:c.933G>C	ENSP00000455848.2:p.Ala311=
ENST00000552678.2:c.933G>C	ENSP00000457394.2:p.Ala311=
ENST00000388922.9:c.933G>C MANE Select	ENSP00000373574.4:p.Ala311=
ENST00000388922.8:c.933G>C	ENSP00000373574.4:p.Ala311=
ENST00000419526.6:c.411G>C	ENSP00000392492.2:p.Ala137=
ENST00000550683.5:c.975G>C	ENSP00000447884.1:p.Ala325=
NM_000020.2:c.933G>C , LRG_543t1:c.933G>C	NP_000011.2:p.Ala311=
NM_001077401.1:c.933G>C	NP_001070869.1:p.Ala311=
XM_005269235.2:c.933G>C	XP_005269292.1:p.Ala311=
XM_011539008.1:c.663G>C	XP_011537310.1:p.Ala221=
XM_024449279.1:c.144G>C	XP_024305047.1:p.Ala48=
NM_000020.3:c.933G>C MANE Select	NP_000011.2:p.Ala311=
NM_001077401.2:c.933G>C	NP_001070869.1:p.Ala311=