Canonical Allele Identifier: CA384899958

Gene: ACVRL1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51914445G>T , CM000674.2:g.51914445G>T	GRCh38
NC_000012.11:g.52308229G>T , CM000674.1:g.52308229G>T	GRCh37
NC_000012.10:g.50594496G>T	NCBI36
NG_009549.1:g.12028G>T , LRG_543:g.12028G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000020.3:c.632G>T MANE Select	NP_000011.2:p.Gly211Val
ENST00000388922.9:c.632G>T MANE Select	ENSP00000373574.4:p.Gly211Val
NM_000020.2:c.632G>T , LRG_543t1:c.632G>T	NP_000011.2:p.Gly211Val
NM_001077401.1:c.632G>T	NP_001070869.1:p.Gly211Val
NM_001077401.2:c.632G>T	NP_001070869.1:p.Gly211Val
ENST00000388922.8:c.632G>T	ENSP00000373574.4:p.Gly211Val
ENST00000419526.6:c.110G>T	ENSP00000392492.2:p.Gly37Val
ENST00000547400.5:c.362G>T	ENSP00000446724.1:p.Gly121Val
ENST00000547400.6:c.362G>T	ENSP00000446724.2:p.Gly121Val
ENST00000550683.5:c.674G>T	ENSP00000447884.1:p.Gly225Val
ENST00000551576.6:c.632G>T	ENSP00000455848.2:p.Gly211Val
ENST00000552678.2:c.632G>T	ENSP00000457394.2:p.Gly211Val
XM_005269235.2:c.632G>T	XP_005269292.1:p.Gly211Val
XM_011539008.1:c.362G>T	XP_011537310.1:p.Gly121Val
XM_024449279.1:c.-158G>T	XP_024305047.1:n.-158G>T