Canonical Allele Identifier: CA270762

Gene: ACVRL1

Linked Data

• ClinVar Variation Id: 156349
• ClinVar RCV Id: RCV000144433
• dbSNP Id: rs267606633
• MyVariant Identifiers: chr12:g.52306966G>C (hg19) ; chr12:g.51913182G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51913182G>C , CM000674.2:g.51913182G>C	GRCh38
NC_000012.11:g.52306966G>C , CM000674.1:g.52306966G>C	GRCh37
NC_000012.10:g.50593233G>C	NCBI36
NG_009549.1:g.10765G>C , LRG_543:g.10765G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000547400.6:c.187G>C	ENSP00000446724.2:p.Ala63Pro
ENST00000551576.6:c.145G>C	ENSP00000455848.2:p.Ala49Pro
ENST00000552678.2:c.145G>C	ENSP00000457394.2:p.Ala49Pro
ENST00000388922.9:c.145G>C MANE Select	ENSP00000373574.4:p.Ala49Pro
ENST00000388922.8:c.145G>C	ENSP00000373574.4:p.Ala49Pro
ENST00000419526.6:c.103+647G>C	ENSP00000392492.2:n.103+647G>C
ENST00000547400.5:c.187G>C	ENSP00000446724.1:p.Ala63Pro
ENST00000550683.5:c.187G>C	ENSP00000447884.1:p.Ala63Pro
ENST00000551576.5:c.145G>C	ENSP00000455848.1:p.Ala49Pro
NM_000020.2:c.145G>C , LRG_543t1:c.145G>C	NP_000011.2:p.Ala49Pro
NM_001077401.1:c.145G>C	NP_001070869.1:p.Ala49Pro
XM_005269235.2:c.145G>C	XP_005269292.1:p.Ala49Pro
XM_011539008.1:c.187G>C	XP_011537310.1:p.Ala63Pro
NM_000020.3:c.145G>C MANE Select	NP_000011.2:p.Ala49Pro
NM_001077401.2:c.145G>C	NP_001070869.1:p.Ala49Pro