Canonical Allele Identifier: CA480063154

Gene: ACVRL1

Linked Data

• ClinVar Variation Id: 1590679
• ClinVar RCV Id: RCV002103742
• dbSNP Id: rs543884349
• gnomAD v2: 12-52309049-G-T
• gnomAD v3: 12-51915265-G-T
• gnomAD v4: 12-51915265-G-T
• MyVariant Identifiers: chr12:g.52309049G>T (hg19) ; chr12:g.51915265G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51915265G>T , CM000674.2:g.51915265G>T	GRCh38
NC_000012.11:g.52309049G>T , CM000674.1:g.52309049G>T	GRCh37
NC_000012.10:g.50595316G>T	NCBI36
NG_009549.1:g.12848G>T , LRG_543:g.12848G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547400.6:c.543G>T	ENSP00000446724.2:p.Thr181=
ENST00000551576.6:c.813G>T	ENSP00000455848.2:p.Thr271=
ENST00000552678.2:c.813G>T	ENSP00000457394.2:p.Thr271=
ENST00000388922.9:c.813G>T MANE Select	ENSP00000373574.4:p.Thr271=
ENST00000388922.8:c.813G>T	ENSP00000373574.4:p.Thr271=
ENST00000419526.6:c.291G>T	ENSP00000392492.2:p.Thr97=
ENST00000550683.5:c.855G>T	ENSP00000447884.1:p.Thr285=
NM_000020.2:c.813G>T , LRG_543t1:c.813G>T	NP_000011.2:p.Thr271=
NM_001077401.1:c.813G>T	NP_001070869.1:p.Thr271=
XM_005269235.2:c.813G>T	XP_005269292.1:p.Thr271=
XM_011539008.1:c.543G>T	XP_011537310.1:p.Thr181=
XM_024449279.1:c.24G>T	XP_024305047.1:p.Thr8=
NM_000020.3:c.813G>T MANE Select	NP_000011.2:p.Thr271=
NM_001077401.2:c.813G>T	NP_001070869.1:p.Thr271=