Canonical Allele Identifier: CA236362556

Gene: ACVRL1

Linked Data

• dbSNP Id: rs948831950
• gnomAD v2: 12-52307517-T-C
• gnomAD v3: 12-51913733-T-C
• gnomAD v4: 12-51913733-T-C
• MyVariant Identifiers: chr12:g.52307517T>C (hg19) ; chr12:g.51913733T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51913733T>C , CM000674.2:g.51913733T>C	GRCh38
NC_000012.11:g.52307517T>C , CM000674.1:g.52307517T>C	GRCh37
NC_000012.10:g.50593784T>C	NCBI36
NG_009549.1:g.11316T>C , LRG_543:g.11316T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547400.6:c.355+383T>C	ENSP00000446724.2:n.355+383T>C
ENST00000551576.6:c.488T>C	ENSP00000455848.2:p.Ile163Thr
ENST00000552678.2:c.488T>C	ENSP00000457394.2:p.Ile163Thr
ENST00000388922.9:c.488T>C MANE Select	ENSP00000373574.4:p.Ile163Thr
ENST00000388922.8:c.488T>C	ENSP00000373574.4:p.Ile163Thr
ENST00000419526.6:c.104-706T>C	ENSP00000392492.2:n.104-706T>C
ENST00000547400.5:c.355+383T>C	ENSP00000446724.1:n.355+383T>C
ENST00000550683.5:c.530T>C	ENSP00000447884.1:p.Ile177Thr
NM_000020.2:c.488T>C , LRG_543t1:c.488T>C	NP_000011.2:p.Ile163Thr
NM_001077401.1:c.488T>C	NP_001070869.1:p.Ile163Thr
XM_005269235.2:c.488T>C	XP_005269292.1:p.Ile163Thr
XM_011539008.1:c.355+383T>C	XP_011537310.1:n.355+383T>C
XM_024449279.1:c.-202T>C	XP_024305047.1:n.-202T>C
NM_000020.3:c.488T>C MANE Select	NP_000011.2:p.Ile163Thr
NM_001077401.2:c.488T>C	NP_001070869.1:p.Ile163Thr