Canonical Allele Identifier: CA384896155

Gene: ACVRL1

Linked Data

• MyVariant Identifiers: chr12:g.52306227C>A (hg19) ; chr12:g.51912443C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51912443C>A , CM000674.2:g.51912443C>A	GRCh38
NC_000012.11:g.52306227C>A , CM000674.1:g.52306227C>A	GRCh37
NC_000012.10:g.50592494C>A	NCBI36
NG_009549.1:g.10026C>A , LRG_543:g.10026C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547400.6:c.11C>A	ENSP00000446724.2:p.Thr4Asn
ENST00000551576.6:c.-5-27C>A	ENSP00000455848.2:n.-5-27C>A
ENST00000552678.2:c.-5-27C>A	ENSP00000457394.2:n.-5-27C>A
ENST00000388922.9:c.-5-27C>A MANE Select	ENSP00000373574.4:n.-5-27C>A
ENST00000388922.8:c.-5-27C>A	ENSP00000373574.4:n.-5-27C>A
ENST00000419526.6:c.11C>A	ENSP00000392492.2:p.Thr4Asn
ENST00000547400.5:c.11C>A	ENSP00000446724.1:p.Thr4Asn
ENST00000550683.5:c.11C>A	ENSP00000447884.1:p.Thr4Asn
ENST00000551576.5:c.-5-27C>A	ENSP00000455848.1:n.-5-27C>A
NM_000020.2:c.-5-27C>A , LRG_543t1:c.-5-27C>A	NP_000011.2:n.-5-27C>A
NM_001077401.1:c.-32C>A	NP_001070869.1:n.-32C>A
XM_005269235.2:c.-5-27C>A	XP_005269292.1:n.-5-27C>A
XM_011539008.1:c.11C>A	XP_011537310.1:p.Thr4Asn
NM_000020.3:c.-5-27C>A MANE Select	NP_000011.2:n.-5-27C>A
NM_001077401.2:c.-32C>A	NP_001070869.1:n.-32C>A