Canonical Allele Identifier: CA384902589

Gene: ACVRL1

Linked Data

• ClinVar Variation Id: 533347
• ClinVar RCV Id: RCV000640440
• dbSNP Id: rs148057374
• MyVariant Identifiers: chr12:g.52309918G>T (hg19) ; chr12:g.51916134G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51916134G>T , CM000674.2:g.51916134G>T	GRCh38
NC_000012.11:g.52309918G>T , CM000674.1:g.52309918G>T	GRCh37
NC_000012.10:g.50596185G>T	NCBI36
NG_009549.1:g.13717G>T , LRG_543:g.13717G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547400.6:c.877G>T	ENSP00000446724.2:p.Glu293Ter
ENST00000551576.6:c.1147G>T	ENSP00000455848.2:p.Glu383Ter
ENST00000552678.2:c.1147G>T	ENSP00000457394.2:p.Glu383Ter
ENST00000388922.9:c.1147G>T MANE Select	ENSP00000373574.4:p.Glu383Ter
ENST00000388922.8:c.1147G>T	ENSP00000373574.4:p.Glu383Ter
ENST00000419526.6:c.625G>T	ENSP00000392492.2:p.Glu209Ter
ENST00000547632.1:n.422G>T
ENST00000550683.5:c.1189G>T	ENSP00000447884.1:p.Glu397Ter
ENST00000552678.1:c.152G>T
NM_000020.2:c.1147G>T , LRG_543t1:c.1147G>T	NP_000011.2:p.Glu383Ter
NM_001077401.1:c.1147G>T	NP_001070869.1:p.Glu383Ter
XM_005269235.2:c.1147G>T	XP_005269292.1:p.Glu383Ter
XM_011539008.1:c.877G>T	XP_011537310.1:p.Glu293Ter
XM_024449279.1:c.358G>T	XP_024305047.1:p.Glu120Ter
NM_000020.3:c.1147G>T MANE Select	NP_000011.2:p.Glu383Ter
NM_001077401.2:c.1147G>T	NP_001070869.1:p.Glu383Ter