Canonical Allele Identifier: CA2036269442

Gene: ACVRL1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51915286C= , CM000674.2:g.51915286C=	GRCh38
NC_000012.11:g.52309070C= , CM000674.1:g.52309070C=	GRCh37
NC_000012.10:g.50595337C=	NCBI36
NG_009549.1:g.12869C= , LRG_543:g.12869C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000547400.6:c.564C=	ENSP00000446724.2:p.His188=
ENST00000551576.6:c.834C=	ENSP00000455848.2:p.His278=
ENST00000552678.2:c.834C=	ENSP00000457394.2:p.His278=
ENST00000388922.9:c.834C= MANE Select	ENSP00000373574.4:p.His278=
ENST00000388922.8:c.834C=	ENSP00000373574.4:p.His278=
ENST00000419526.6:c.312C=	ENSP00000392492.2:p.His104=
ENST00000550683.5:c.876C=	ENSP00000447884.1:p.His292=
NM_000020.2:c.834C= , LRG_543t1:c.834C=	NP_000011.2:p.His278=
NM_001077401.1:c.834C=	NP_001070869.1:p.His278=
XM_005269235.2:c.834C=	XP_005269292.1:p.His278=
XM_011539008.1:c.564C=	XP_011537310.1:p.His188=
XM_024449279.1:c.45C=	XP_024305047.1:p.His15=
NM_000020.3:c.834C= MANE Select	NP_000011.2:p.His278=
NM_001077401.2:c.834C=	NP_001070869.1:p.His278=