Canonical Allele Identifier: CA480063165

Gene: ACVRL1

Linked Data

• gnomAD v4: 12-51915289-C-T
• MyVariant Identifiers: chr12:g.52309073C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51915289C>T , CM000674.2:g.51915289C>T	GRCh38
NC_000012.11:g.52309073C>T , CM000674.1:g.52309073C>T	GRCh37
NC_000012.10:g.50595340C>T	NCBI36
NG_009549.1:g.12872C>T , LRG_543:g.12872C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000547400.6:c.567C>T	ENSP00000446724.2:p.Tyr189=
ENST00000551576.6:c.837C>T	ENSP00000455848.2:p.Tyr279=
ENST00000552678.2:c.837C>T	ENSP00000457394.2:p.Tyr279=
ENST00000388922.9:c.837C>T MANE Select	ENSP00000373574.4:p.Tyr279=
ENST00000388922.8:c.837C>T	ENSP00000373574.4:p.Tyr279=
ENST00000419526.6:c.315C>T	ENSP00000392492.2:p.Tyr105=
ENST00000550683.5:c.879C>T	ENSP00000447884.1:p.Tyr293=
NM_000020.2:c.837C>T , LRG_543t1:c.837C>T	NP_000011.2:p.Tyr279=
NM_001077401.1:c.837C>T	NP_001070869.1:p.Tyr279=
XM_005269235.2:c.837C>T	XP_005269292.1:p.Tyr279=
XM_011539008.1:c.567C>T	XP_011537310.1:p.Tyr189=
XM_024449279.1:c.48C>T	XP_024305047.1:p.Tyr16=
NM_000020.3:c.837C>T MANE Select	NP_000011.2:p.Tyr279=
NM_001077401.2:c.837C>T	NP_001070869.1:p.Tyr279=