Canonical Allele Identifier: CA384902951

Gene: ACVRL1

Linked Data

• ClinVar Variation Id: 1749360
• ClinVar RCV Id: RCV002347760
• MyVariant Identifiers: chr12:g.52309979T>C (hg19) ; chr12:g.51916195T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51916195T>C , CM000674.2:g.51916195T>C	GRCh38
NC_000012.11:g.52309979T>C , CM000674.1:g.52309979T>C	GRCh37
NC_000012.10:g.50596246T>C	NCBI36
NG_009549.1:g.13778T>C , LRG_543:g.13778T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000547400.6:c.938T>C	ENSP00000446724.2:p.Leu313Pro
ENST00000551576.6:c.1208T>C	ENSP00000455848.2:p.Leu403Pro
ENST00000552678.2:c.1208T>C	ENSP00000457394.2:p.Leu403Pro
ENST00000388922.9:c.1208T>C MANE Select	ENSP00000373574.4:p.Leu403Pro
ENST00000388922.8:c.1208T>C	ENSP00000373574.4:p.Leu403Pro
ENST00000419526.6:c.686T>C	ENSP00000392492.2:p.Leu229Pro
ENST00000547632.1:n.483T>C
ENST00000550683.5:c.1250T>C	ENSP00000447884.1:p.Leu417Pro
ENST00000552678.1:c.213T>C
NM_000020.2:c.1208T>C , LRG_543t1:c.1208T>C	NP_000011.2:p.Leu403Pro
NM_001077401.1:c.1208T>C	NP_001070869.1:p.Leu403Pro
XM_005269235.2:c.1208T>C	XP_005269292.1:p.Leu403Pro
XM_011539008.1:c.938T>C	XP_011537310.1:p.Leu313Pro
XM_024449279.1:c.419T>C	XP_024305047.1:p.Leu140Pro
NM_000020.3:c.1208T>C MANE Select	NP_000011.2:p.Leu403Pro
NM_001077401.2:c.1208T>C	NP_001070869.1:p.Leu403Pro