Canonical Allele Identifier: CA2036236965

Gene: ACVRL1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51916133C= , CM000674.2:g.51916133C=	GRCh38
NC_000012.11:g.52309917C= , CM000674.1:g.52309917C=	GRCh37
NC_000012.10:g.50596184C=	NCBI36
NG_009549.1:g.13716C= , LRG_543:g.13716C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547400.6:c.876C=	ENSP00000446724.2:p.Asp292=
ENST00000551576.6:c.1146C=	ENSP00000455848.2:p.Asp382=
ENST00000552678.2:c.1146C=	ENSP00000457394.2:p.Asp382=
ENST00000388922.9:c.1146C= MANE Select	ENSP00000373574.4:p.Asp382=
ENST00000388922.8:c.1146C=	ENSP00000373574.4:p.Asp382=
ENST00000419526.6:c.624C=	ENSP00000392492.2:p.Asp208=
ENST00000547632.1:n.421C=
ENST00000550683.5:c.1188C=	ENSP00000447884.1:p.Asp396=
ENST00000552678.1:c.151C=
NM_000020.2:c.1146C= , LRG_543t1:c.1146C=	NP_000011.2:p.Asp382=
NM_001077401.1:c.1146C=	NP_001070869.1:p.Asp382=
XM_005269235.2:c.1146C=	XP_005269292.1:p.Asp382=
XM_011539008.1:c.876C=	XP_011537310.1:p.Asp292=
XM_024449279.1:c.357C=	XP_024305047.1:p.Asp119=
NM_000020.3:c.1146C= MANE Select	NP_000011.2:p.Asp382=
NM_001077401.2:c.1146C=	NP_001070869.1:p.Asp382=