Canonical Allele Identifier: CA384900054

Gene: ACVRL1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51914490T>A , CM000674.2:g.51914490T>A	GRCh38
NC_000012.11:g.52308274T>A , CM000674.1:g.52308274T>A	GRCh37
NC_000012.10:g.50594541T>A	NCBI36
NG_009549.1:g.12073T>A , LRG_543:g.12073T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547400.6:c.407T>A	ENSP00000446724.2:p.Val136Glu
ENST00000551576.6:c.677T>A	ENSP00000455848.2:p.Val226Glu
ENST00000552678.2:c.677T>A	ENSP00000457394.2:p.Val226Glu
ENST00000388922.9:c.677T>A MANE Select	ENSP00000373574.4:p.Val226Glu
ENST00000388922.8:c.677T>A	ENSP00000373574.4:p.Val226Glu
ENST00000419526.6:c.155T>A	ENSP00000392492.2:p.Val52Glu
ENST00000547400.5:c.407T>A	ENSP00000446724.1:p.Val136Glu
ENST00000550683.5:c.719T>A	ENSP00000447884.1:p.Val240Glu
NM_000020.2:c.677T>A , LRG_543t1:c.677T>A	NP_000011.2:p.Val226Glu
NM_001077401.1:c.677T>A	NP_001070869.1:p.Val226Glu
XM_005269235.2:c.677T>A	XP_005269292.1:p.Val226Glu
XM_011539008.1:c.407T>A	XP_011537310.1:p.Val136Glu
XM_024449279.1:c.-113T>A	XP_024305047.1:n.-113T>A
NM_000020.3:c.677T>A MANE Select	NP_000011.2:p.Val226Glu
NM_001077401.2:c.677T>A	NP_001070869.1:p.Val226Glu