Canonical Allele Identifier: CA16614039

Gene: ACVRL1

Linked Data

• ClinVar Variation Id: 411299
• ClinVar RCV Id: RCV000475892 ; RCV003221991 ; RCV004551532
• dbSNP Id: rs1060503234
• gnomAD v4: 12-51913303-G-T
• MyVariant Identifiers: chr12:g.52307087G>T (hg19) ; chr12:g.51913303G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51913303G>T , CM000674.2:g.51913303G>T	GRCh38
NC_000012.11:g.52307087G>T , CM000674.1:g.52307087G>T	GRCh37
NC_000012.10:g.50593354G>T	NCBI36
NG_009549.1:g.10886G>T , LRG_543:g.10886G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547400.6:c.308G>T	ENSP00000446724.2:p.Cys103Phe
ENST00000551576.6:c.266G>T	ENSP00000455848.2:p.Cys89Phe
ENST00000552678.2:c.266G>T	ENSP00000457394.2:p.Cys89Phe
ENST00000388922.9:c.266G>T MANE Select	ENSP00000373574.4:p.Cys89Phe
ENST00000388922.8:c.266G>T	ENSP00000373574.4:p.Cys89Phe
ENST00000419526.6:c.103+768G>T	ENSP00000392492.2:n.103+768G>T
ENST00000547400.5:c.308G>T	ENSP00000446724.1:p.Cys103Phe
ENST00000550683.5:c.308G>T	ENSP00000447884.1:p.Cys103Phe
ENST00000551576.5:c.266G>T	ENSP00000455848.1:p.Cys89Phe
NM_000020.2:c.266G>T , LRG_543t1:c.266G>T	NP_000011.2:p.Cys89Phe
NM_001077401.1:c.266G>T	NP_001070869.1:p.Cys89Phe
XM_005269235.2:c.266G>T	XP_005269292.1:p.Cys89Phe
XM_011539008.1:c.308G>T	XP_011537310.1:p.Cys103Phe
XM_024449279.1:c.-424G>T	XP_024305047.1:n.-424G>T
NM_000020.3:c.266G>T MANE Select	NP_000011.2:p.Cys89Phe
NM_001077401.2:c.266G>T	NP_001070869.1:p.Cys89Phe