Canonical Allele Identifier: CA479817042

Gene: ACVRL1

Linked Data

• MyVariant Identifiers: chr12:g.52314632A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51920848A>T , CM000674.2:g.51920848A>T	GRCh38
NC_000012.11:g.52314632A>T , CM000674.1:g.52314632A>T	GRCh37
NC_000012.10:g.50600899A>T	NCBI36
NG_009549.1:g.18431A>T , LRG_543:g.18431A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000547400.6:c.1197A>T	ENSP00000446724.2:p.Leu399=
ENST00000551576.6:c.1467A>T	ENSP00000455848.2:p.Leu489=
ENST00000388922.9:c.1467A>T MANE Select	ENSP00000373574.4:p.Leu489=
ENST00000388922.8:c.1467A>T	ENSP00000373574.4:p.Leu489=
ENST00000419526.6:c.945A>T	ENSP00000392492.2:p.Leu315=
ENST00000550683.5:c.1509A>T	ENSP00000447884.1:p.Leu503=
NM_000020.2:c.1467A>T , LRG_543t1:c.1467A>T	NP_000011.2:p.Leu489=
NM_001077401.1:c.1467A>T	NP_001070869.1:p.Leu489=
XM_005269235.2:c.1467A>T	XP_005269292.1:p.Leu489=
XM_011539008.1:c.1197A>T	XP_011537310.1:p.Leu399=
XM_024449279.1:c.678A>T	XP_024305047.1:p.Leu226=
NM_000020.3:c.1467A>T MANE Select	NP_000011.2:p.Leu489=
NM_001077401.2:c.1467A>T	NP_001070869.1:p.Leu489=