Canonical Allele Identifier: CA605053088

Gene: ACVRL1

Linked Data

• dbSNP Id: rs1359569568
• gnomAD v2: 12-52314689-C-T
• MyVariant Identifiers: chr12:g.52314689C>T (hg19) ; chr12:g.51920905C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51920905C>T , CM000674.2:g.51920905C>T	GRCh38
NC_000012.11:g.52314689C>T , CM000674.1:g.52314689C>T	GRCh37
NC_000012.10:g.50600956C>T	NCBI36
NG_009549.1:g.18488C>T , LRG_543:g.18488C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000551576.6:c.*12C>T	ENSP00000455848.2:n.*12C>T
ENST00000388922.9:c.*12C>T MANE Select	ENSP00000373574.4:n.*12C>T
ENST00000388922.8:c.*12C>T	ENSP00000373574.4:n.*12C>T
ENST00000419526.6:c.*12C>T	ENSP00000392492.2:n.*12C>T
ENST00000550683.5:c.*12C>T	ENSP00000447884.1:n.*12C>T
NM_000020.2:c.*12C>T , LRG_543t1:c.*12C>T	NP_000011.2:n.*12C>T
NM_001077401.1:c.*12C>T	NP_001070869.1:n.*12C>T
XM_005269235.2:c.*12C>T	XP_005269292.1:n.*12C>T
XM_011539008.1:c.*12C>T	XP_011537310.1:n.*12C>T
XM_024449279.1:c.*12C>T	XP_024305047.1:n.*12C>T
NM_000020.3:c.*12C>T MANE Select	NP_000011.2:n.*12C>T
NM_001077401.2:c.*12C>T	NP_001070869.1:n.*12C>T