Canonical Allele Identifier: CA2036267886

Gene: ACVRL1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51913668G= , CM000674.2:g.51913668G=	GRCh38
NC_000012.11:g.52307452G= , CM000674.1:g.52307452G=	GRCh37
NC_000012.10:g.50593719G=	NCBI36
NG_009549.1:g.11251G= , LRG_543:g.11251G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547400.6:c.355+318G=	ENSP00000446724.2:n.355+318G=
ENST00000551576.6:c.423G=	ENSP00000455848.2:p.Trp141=
ENST00000552678.2:c.423G=	ENSP00000457394.2:p.Trp141=
ENST00000388922.9:c.423G= MANE Select	ENSP00000373574.4:p.Trp141=
ENST00000388922.8:c.423G=	ENSP00000373574.4:p.Trp141=
ENST00000419526.6:c.104-771G=	ENSP00000392492.2:n.104-771G=
ENST00000547400.5:c.355+318G=	ENSP00000446724.1:n.355+318G=
ENST00000550683.5:c.465G=	ENSP00000447884.1:p.Trp155=
NM_000020.2:c.423G= , LRG_543t1:c.423G=	NP_000011.2:p.Trp141=
NM_001077401.1:c.423G=	NP_001070869.1:p.Trp141=
XM_005269235.2:c.423G=	XP_005269292.1:p.Trp141=
XM_011539008.1:c.355+318G=	XP_011537310.1:n.355+318G=
XM_024449279.1:c.-267G=	XP_024305047.1:n.-267G=
NM_000020.3:c.423G= MANE Select	NP_000011.2:p.Trp141=
NM_001077401.2:c.423G=	NP_001070869.1:p.Trp141=