Canonical Allele Identifier: CA2036266015

Gene: ACVRL1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51912340A= , CM000674.2:g.51912340A=	GRCh38
NC_000012.11:g.52306124A= , CM000674.1:g.52306124A=	GRCh37
NC_000012.10:g.50592391A=	NCBI36
NG_009549.1:g.9923A= , LRG_543:g.9923A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547400.6:c.-93A=	ENSP00000446724.2:n.-93A=
ENST00000551576.6:c.-5-130A=	ENSP00000455848.2:n.-5-130A=
ENST00000552678.2:c.-5-130A=	ENSP00000457394.2:n.-5-130A=
ENST00000388922.9:c.-5-130A= MANE Select	ENSP00000373574.4:n.-5-130A=
ENST00000388922.8:c.-5-130A=	ENSP00000373574.4:n.-5-130A=
ENST00000547400.5:c.-93A=	ENSP00000446724.1:n.-93A=
ENST00000550683.5:c.-93A=	ENSP00000447884.1:n.-93A=
ENST00000551576.5:c.-5-130A=	ENSP00000455848.1:n.-5-130A=
NM_000020.2:c.-5-130A= , LRG_543t1:c.-5-130A=	NP_000011.2:n.-5-130A=
NM_001077401.1:c.-135A=	NP_001070869.1:n.-135A=
XM_005269235.2:c.-5-130A=	XP_005269292.1:n.-5-130A=
XM_011539008.1:c.-93A=	XP_011537310.1:n.-93A=
NM_000020.3:c.-5-130A= MANE Select	NP_000011.2:n.-5-130A=