Canonical Allele Identifier: CA2036242297

Gene: ACVRL1

Linked Data

• dbSNP Id: rs1940970233
• gnomAD v4: 12-51921127-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51921127C>T , CM000674.2:g.51921127C>T	GRCh38
NC_000012.11:g.52314911C>T , CM000674.1:g.52314911C>T	GRCh37
NC_000012.10:g.50601178C>T	NCBI36
NG_009549.1:g.18710C>T , LRG_543:g.18710C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000551576.6:c.*234C>T	ENSP00000455848.2:n.*234C>T
ENST00000388922.9:c.*234C>T MANE Select	ENSP00000373574.4:n.*234C>T
ENST00000419526.6:c.*234C>T	ENSP00000392492.2:n.*234C>T
ENST00000550683.5:c.*234C>T	ENSP00000447884.1:n.*234C>T
NM_000020.2:c.*234C>T , LRG_543t1:c.*234C>T	NP_000011.2:n.*234C>T
NM_001077401.1:c.*234C>T	NP_001070869.1:n.*234C>T
XM_005269235.2:c.*234C>T	XP_005269292.1:n.*234C>T
XM_011539008.1:c.*234C>T	XP_011537310.1:n.*234C>T
XM_024449279.1:c.*234C>T	XP_024305047.1:n.*234C>T
NM_000020.3:c.*234C>T MANE Select	NP_000011.2:n.*234C>T
NM_001077401.2:c.*234C>T	NP_001070869.1:n.*234C>T