Canonical Allele Identifier: CA384900376

Gene: ACVRL1

Linked Data

• MyVariant Identifiers: chr12:g.52309038A>C (hg19) ; chr12:g.51915254A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51915254A>C , CM000674.2:g.51915254A>C	GRCh38
NC_000012.11:g.52309038A>C , CM000674.1:g.52309038A>C	GRCh37
NC_000012.10:g.50595305A>C	NCBI36
NG_009549.1:g.12837A>C , LRG_543:g.12837A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547400.6:c.532A>C	ENSP00000446724.2:p.Asn178His
ENST00000551576.6:c.802A>C	ENSP00000455848.2:p.Asn268His
ENST00000552678.2:c.802A>C	ENSP00000457394.2:p.Asn268His
ENST00000388922.9:c.802A>C MANE Select	ENSP00000373574.4:p.Asn268His
ENST00000388922.8:c.802A>C	ENSP00000373574.4:p.Asn268His
ENST00000419526.6:c.280A>C	ENSP00000392492.2:p.Asn94His
ENST00000550683.5:c.844A>C	ENSP00000447884.1:p.Asn282His
NM_000020.2:c.802A>C , LRG_543t1:c.802A>C	NP_000011.2:p.Asn268His
NM_001077401.1:c.802A>C	NP_001070869.1:p.Asn268His
XM_005269235.2:c.802A>C	XP_005269292.1:p.Asn268His
XM_011539008.1:c.532A>C	XP_011537310.1:p.Asn178His
XM_024449279.1:c.13A>C	XP_024305047.1:p.Asn5His
NM_000020.3:c.802A>C MANE Select	NP_000011.2:p.Asn268His
NM_001077401.2:c.802A>C	NP_001070869.1:p.Asn268His