Canonical Allele Identifier: CA2036268503

Gene: ACVRL1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51914103G= , CM000674.2:g.51914103G=	GRCh38
NC_000012.11:g.52307887G= , CM000674.1:g.52307887G=	GRCh37
NC_000012.10:g.50594154G=	NCBI36
NG_009549.1:g.11686G= , LRG_543:g.11686G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547400.6:c.356-336G=	ENSP00000446724.2:n.356-336G=
ENST00000551576.6:c.625+30G=	ENSP00000455848.2:n.625+30G=
ENST00000552678.2:c.625+30G=	ENSP00000457394.2:n.625+30G=
ENST00000388922.9:c.625+30G= MANE Select	ENSP00000373574.4:n.625+30G=
ENST00000388922.8:c.625+30G=	ENSP00000373574.4:n.625+30G=
ENST00000419526.6:c.104-336G=	ENSP00000392492.2:n.104-336G=
ENST00000547400.5:c.356-336G=	ENSP00000446724.1:n.356-336G=
ENST00000550683.5:c.667+30G=	ENSP00000447884.1:n.667+30G=
NM_000020.2:c.625+30G= , LRG_543t1:c.625+30G=	NP_000011.2:n.625+30G=
NM_001077401.1:c.625+30G=	NP_001070869.1:n.625+30G=
XM_005269235.2:c.625+30G=	XP_005269292.1:n.625+30G=
XM_011539008.1:c.356-336G=	XP_011537310.1:n.356-336G=
XM_024449279.1:c.-165+333G=	XP_024305047.1:n.-165+333G=
NM_000020.3:c.625+30G= MANE Select	NP_000011.2:n.625+30G=
NM_001077401.2:c.625+30G=	NP_001070869.1:n.625+30G=