Canonical Allele Identifier: CA384899967

Gene: ACVRL1

Linked Data

• MyVariant Identifiers: chr12:g.52308234T>G (hg19) ; chr12:g.51914450T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51914450T>G , CM000674.2:g.51914450T>G	GRCh38
NC_000012.11:g.52308234T>G , CM000674.1:g.52308234T>G	GRCh37
NC_000012.10:g.50594501T>G	NCBI36
NG_009549.1:g.12033T>G , LRG_543:g.12033T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000547400.6:c.367T>G	ENSP00000446724.2:p.Tyr123Asp
ENST00000551576.6:c.637T>G	ENSP00000455848.2:p.Tyr213Asp
ENST00000552678.2:c.637T>G	ENSP00000457394.2:p.Tyr213Asp
ENST00000388922.9:c.637T>G MANE Select	ENSP00000373574.4:p.Tyr213Asp
ENST00000388922.8:c.637T>G	ENSP00000373574.4:p.Tyr213Asp
ENST00000419526.6:c.115T>G	ENSP00000392492.2:p.Tyr39Asp
ENST00000547400.5:c.367T>G	ENSP00000446724.1:p.Tyr123Asp
ENST00000550683.5:c.679T>G	ENSP00000447884.1:p.Tyr227Asp
NM_000020.2:c.637T>G , LRG_543t1:c.637T>G	NP_000011.2:p.Tyr213Asp
NM_001077401.1:c.637T>G	NP_001070869.1:p.Tyr213Asp
XM_005269235.2:c.637T>G	XP_005269292.1:p.Tyr213Asp
XM_011539008.1:c.367T>G	XP_011537310.1:p.Tyr123Asp
XM_024449279.1:c.-153T>G	XP_024305047.1:n.-153T>G
NM_000020.3:c.637T>G MANE Select	NP_000011.2:p.Tyr213Asp
NM_001077401.2:c.637T>G	NP_001070869.1:p.Tyr213Asp