Canonical Allele Identifier: CA479817217

Gene: ACVRL1

Linked Data

• MyVariant Identifiers: chr12:g.52314653A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51920869A>C , CM000674.2:g.51920869A>C	GRCh38
NC_000012.11:g.52314653A>C , CM000674.1:g.52314653A>C	GRCh37
NC_000012.10:g.50600920A>C	NCBI36
NG_009549.1:g.18452A>C , LRG_543:g.18452A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547400.6:c.1218A>C	ENSP00000446724.2:p.Pro406=
ENST00000551576.6:c.1488A>C	ENSP00000455848.2:p.Pro496=
ENST00000388922.9:c.1488A>C MANE Select	ENSP00000373574.4:p.Pro496=
ENST00000388922.8:c.1488A>C	ENSP00000373574.4:p.Pro496=
ENST00000419526.6:c.966A>C	ENSP00000392492.2:p.Pro322=
ENST00000550683.5:c.1530A>C	ENSP00000447884.1:p.Pro510=
NM_000020.2:c.1488A>C , LRG_543t1:c.1488A>C	NP_000011.2:p.Pro496=
NM_001077401.1:c.1488A>C	NP_001070869.1:p.Pro496=
XM_005269235.2:c.1488A>C	XP_005269292.1:p.Pro496=
XM_011539008.1:c.1218A>C	XP_011537310.1:p.Pro406=
XM_024449279.1:c.699A>C	XP_024305047.1:p.Pro233=
NM_000020.3:c.1488A>C MANE Select	NP_000011.2:p.Pro496=
NM_001077401.2:c.1488A>C	NP_001070869.1:p.Pro496=