Canonical Allele Identifier: CA479804824

Gene: ACVRL1

Linked Data

• gnomAD v4: 12-51913653-T-G
• MyVariant Identifiers: chr12:g.52307437T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51913653T>G , CM000674.2:g.51913653T>G	GRCh38
NC_000012.11:g.52307437T>G , CM000674.1:g.52307437T>G	GRCh37
NC_000012.10:g.50593704T>G	NCBI36
NG_009549.1:g.11236T>G , LRG_543:g.11236T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547400.6:c.355+303T>G	ENSP00000446724.2:n.355+303T>G
ENST00000551576.6:c.408T>G	ENSP00000455848.2:p.Gly136=
ENST00000552678.2:c.408T>G	ENSP00000457394.2:p.Gly136=
ENST00000388922.9:c.408T>G MANE Select	ENSP00000373574.4:p.Gly136=
ENST00000388922.8:c.408T>G	ENSP00000373574.4:p.Gly136=
ENST00000419526.6:c.104-786T>G	ENSP00000392492.2:n.104-786T>G
ENST00000547400.5:c.355+303T>G	ENSP00000446724.1:n.355+303T>G
ENST00000550683.5:c.450T>G	ENSP00000447884.1:p.Gly150=
NM_000020.2:c.408T>G , LRG_543t1:c.408T>G	NP_000011.2:p.Gly136=
NM_001077401.1:c.408T>G	NP_001070869.1:p.Gly136=
XM_005269235.2:c.408T>G	XP_005269292.1:p.Gly136=
XM_011539008.1:c.355+303T>G	XP_011537310.1:n.355+303T>G
XM_024449279.1:c.-282T>G	XP_024305047.1:n.-282T>G
NM_000020.3:c.408T>G MANE Select	NP_000011.2:p.Gly136=
NM_001077401.2:c.408T>G	NP_001070869.1:p.Gly136=