Canonical Allele Identifier: CA236363987

Gene: ACVRL1

Linked Data

• dbSNP Id: rs930393044
• gnomAD v4: 12-51915281-A-G
• MyVariant Identifiers: chr12:g.52309065A>G (hg19) ; chr12:g.51915281A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51915281A>G , CM000674.2:g.51915281A>G	GRCh38
NC_000012.11:g.52309065A>G , CM000674.1:g.52309065A>G	GRCh37
NC_000012.10:g.50595332A>G	NCBI36
NG_009549.1:g.12864A>G , LRG_543:g.12864A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000547400.6:c.559A>G	ENSP00000446724.2:p.Thr187Ala
ENST00000551576.6:c.829A>G	ENSP00000455848.2:p.Thr277Ala
ENST00000552678.2:c.829A>G	ENSP00000457394.2:p.Thr277Ala
ENST00000388922.9:c.829A>G MANE Select	ENSP00000373574.4:p.Thr277Ala
ENST00000388922.8:c.829A>G	ENSP00000373574.4:p.Thr277Ala
ENST00000419526.6:c.307A>G	ENSP00000392492.2:p.Thr103Ala
ENST00000550683.5:c.871A>G	ENSP00000447884.1:p.Thr291Ala
NM_000020.2:c.829A>G , LRG_543t1:c.829A>G	NP_000011.2:p.Thr277Ala
NM_001077401.1:c.829A>G	NP_001070869.1:p.Thr277Ala
XM_005269235.2:c.829A>G	XP_005269292.1:p.Thr277Ala
XM_011539008.1:c.559A>G	XP_011537310.1:p.Thr187Ala
XM_024449279.1:c.40A>G	XP_024305047.1:p.Thr14Ala
NM_000020.3:c.829A>G MANE Select	NP_000011.2:p.Thr277Ala
NM_001077401.2:c.829A>G	NP_001070869.1:p.Thr277Ala