Canonical Allele Identifier: CA915948520

Gene: ACVRL1

Linked Data

• ClinVar Variation Id: 743851
• ClinVar RCV Id: RCV003509633
• dbSNP Id: rs1592223042

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51914083G>A , CM000674.2:g.51914083G>A	GRCh38
NC_000012.11:g.52307867G>A , CM000674.1:g.52307867G>A	GRCh37
NC_000012.10:g.50594134G>A	NCBI36
NG_009549.1:g.11666G>A , LRG_543:g.11666G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000547400.6:c.356-356G>A	ENSP00000446724.2:n.356-356G>A
ENST00000551576.6:c.625+10G>A	ENSP00000455848.2:n.625+10G>A
ENST00000552678.2:c.625+10G>A	ENSP00000457394.2:n.625+10G>A
ENST00000388922.9:c.625+10G>A MANE Select	ENSP00000373574.4:n.625+10G>A
ENST00000388922.8:c.625+10G>A	ENSP00000373574.4:n.625+10G>A
ENST00000419526.6:c.104-356G>A	ENSP00000392492.2:n.104-356G>A
ENST00000547400.5:c.356-356G>A	ENSP00000446724.1:n.356-356G>A
ENST00000550683.5:c.667+10G>A	ENSP00000447884.1:n.667+10G>A
NM_000020.2:c.625+10G>A , LRG_543t1:c.625+10G>A	NP_000011.2:n.625+10G>A
NM_001077401.1:c.625+10G>A	NP_001070869.1:n.625+10G>A
XM_005269235.2:c.625+10G>A	XP_005269292.1:n.625+10G>A
XM_011539008.1:c.356-356G>A	XP_011537310.1:n.356-356G>A
XM_024449279.1:c.-165+313G>A	XP_024305047.1:n.-165+313G>A
NM_000020.3:c.625+10G>A MANE Select	NP_000011.2:n.625+10G>A
NM_001077401.2:c.625+10G>A	NP_001070869.1:n.625+10G>A