Canonical Allele Identifier: CA2036268001

Gene: ACVRL1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51913778C= , CM000674.2:g.51913778C=	GRCh38
NC_000012.11:g.52307562C= , CM000674.1:g.52307562C=	GRCh37
NC_000012.10:g.50593829C=	NCBI36
NG_009549.1:g.11361C= , LRG_543:g.11361C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547400.6:c.355+428C=	ENSP00000446724.2:n.355+428C=
ENST00000551576.6:c.525+8C=	ENSP00000455848.2:n.525+8C=
ENST00000552678.2:c.525+8C=	ENSP00000457394.2:n.525+8C=
ENST00000388922.9:c.525+8C= MANE Select	ENSP00000373574.4:n.525+8C=
ENST00000388922.8:c.525+8C=	ENSP00000373574.4:n.525+8C=
ENST00000419526.6:c.104-661C=	ENSP00000392492.2:n.104-661C=
ENST00000547400.5:c.355+428C=	ENSP00000446724.1:n.355+428C=
ENST00000550683.5:c.567+8C=	ENSP00000447884.1:n.567+8C=
NM_000020.2:c.525+8C= , LRG_543t1:c.525+8C=	NP_000011.2:n.525+8C=
NM_001077401.1:c.525+8C=	NP_001070869.1:n.525+8C=
XM_005269235.2:c.525+8C=	XP_005269292.1:n.525+8C=
XM_011539008.1:c.355+428C=	XP_011537310.1:n.355+428C=
XM_024449279.1:c.-165+8C=	XP_024305047.1:n.-165+8C=
NM_000020.3:c.525+8C= MANE Select	NP_000011.2:n.525+8C=
NM_001077401.2:c.525+8C=	NP_001070869.1:n.525+8C=