Canonical Allele Identifier: CA384905340

Gene: ACVRL1

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51920778A>G , CM000674.2:g.51920778A>G	GRCh38
NC_000012.11:g.52314562A>G , CM000674.1:g.52314562A>G	GRCh37
NC_000012.10:g.50600829A>G	NCBI36
NG_009549.1:g.18361A>G , LRG_543:g.18361A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547400.6:c.1127A>G	ENSP00000446724.2:p.Gln376Arg
ENST00000551576.6:c.1397A>G	ENSP00000455848.2:p.Gln466Arg
ENST00000388922.9:c.1397A>G MANE Select	ENSP00000373574.4:p.Gln466Arg
ENST00000388922.8:c.1397A>G	ENSP00000373574.4:p.Gln466Arg
ENST00000419526.6:c.875A>G	ENSP00000392492.2:p.Gln292Arg
ENST00000550683.5:c.1439A>G	ENSP00000447884.1:p.Gln480Arg
NM_000020.2:c.1397A>G , LRG_543t1:c.1397A>G	NP_000011.2:p.Gln466Arg
NM_001077401.1:c.1397A>G	NP_001070869.1:p.Gln466Arg
XM_005269235.2:c.1397A>G	XP_005269292.1:p.Gln466Arg
XM_011539008.1:c.1127A>G	XP_011537310.1:p.Gln376Arg
XM_024449279.1:c.608A>G	XP_024305047.1:p.Gln203Arg
NM_000020.3:c.1397A>G MANE Select	NP_000011.2:p.Gln466Arg
NM_001077401.2:c.1397A>G	NP_001070869.1:p.Gln466Arg