Canonical Allele Identifier: CA384903794

Gene: ACVRL1

Linked Data

• MyVariant Identifiers: chr12:g.52312801G>T (hg19) ; chr12:g.51919017G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51919017G>T , CM000674.2:g.51919017G>T	GRCh38
NC_000012.11:g.52312801G>T , CM000674.1:g.52312801G>T	GRCh37
NC_000012.10:g.50599068G>T	NCBI36
NG_009549.1:g.16600G>T , LRG_543:g.16600G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547400.6:c.1009G>T	ENSP00000446724.2:p.Asp337Tyr
ENST00000551576.6:c.1279G>T	ENSP00000455848.2:p.Asp427Tyr
ENST00000552678.2:c.1279G>T	ENSP00000457394.2:p.Asp427Tyr
ENST00000388922.9:c.1279G>T MANE Select	ENSP00000373574.4:p.Asp427Tyr
ENST00000388922.8:c.1279G>T	ENSP00000373574.4:p.Asp427Tyr
ENST00000419526.6:c.757G>T	ENSP00000392492.2:p.Asp253Tyr
ENST00000547632.1:n.554G>T
ENST00000550683.5:c.1321G>T	ENSP00000447884.1:p.Asp441Tyr
ENST00000552678.1:c.284G>T
NM_000020.2:c.1279G>T , LRG_543t1:c.1279G>T	NP_000011.2:p.Asp427Tyr
NM_001077401.1:c.1279G>T	NP_001070869.1:p.Asp427Tyr
XM_005269235.2:c.1279G>T	XP_005269292.1:p.Asp427Tyr
XM_011539008.1:c.1009G>T	XP_011537310.1:p.Asp337Tyr
XM_024449279.1:c.490G>T	XP_024305047.1:p.Asp164Tyr
NM_000020.3:c.1279G>T MANE Select	NP_000011.2:p.Asp427Tyr
NM_001077401.2:c.1279G>T	NP_001070869.1:p.Asp427Tyr