Canonical Allele Identifier: CA384900292

Gene: ACVRL1

Linked Data

• MyVariant Identifiers: chr12:g.52309012T>A (hg19) ; chr12:g.51915228T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51915228T>A , CM000674.2:g.51915228T>A	GRCh38
NC_000012.11:g.52309012T>A , CM000674.1:g.52309012T>A	GRCh37
NC_000012.10:g.50595279T>A	NCBI36
NG_009549.1:g.12811T>A , LRG_543:g.12811T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547400.6:c.506T>A	ENSP00000446724.2:p.Phe169Tyr
ENST00000551576.6:c.776T>A	ENSP00000455848.2:p.Phe259Tyr
ENST00000552678.2:c.776T>A	ENSP00000457394.2:p.Phe259Tyr
ENST00000388922.9:c.776T>A MANE Select	ENSP00000373574.4:p.Phe259Tyr
ENST00000388922.8:c.776T>A	ENSP00000373574.4:p.Phe259Tyr
ENST00000419526.6:c.254T>A	ENSP00000392492.2:p.Phe85Tyr
ENST00000550683.5:c.818T>A	ENSP00000447884.1:p.Phe273Tyr
NM_000020.2:c.776T>A , LRG_543t1:c.776T>A	NP_000011.2:p.Phe259Tyr
NM_001077401.1:c.776T>A	NP_001070869.1:p.Phe259Tyr
XM_005269235.2:c.776T>A	XP_005269292.1:p.Phe259Tyr
XM_011539008.1:c.506T>A	XP_011537310.1:p.Phe169Tyr
XM_024449279.1:c.-14T>A	XP_024305047.1:n.-14T>A
NM_000020.3:c.776T>A MANE Select	NP_000011.2:p.Phe259Tyr
NM_001077401.2:c.776T>A	NP_001070869.1:p.Phe259Tyr