Canonical Allele Identifier: CA6572885

Gene: ACVRL1

Linked Data

• ClinVar Variation Id: 2965106
• ClinVar RCV Id: RCV003823272
• dbSNP Id: rs559185621
• ExAC: 12:52307330 C / T
• gnomAD v2: 12-52307330-C-T
• gnomAD v3: 12-51913546-C-T
• gnomAD v4: 12-51913546-C-T
• MyVariant Identifiers: chr12:g.52307330C>T (hg19) ; chr12:g.51913546C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.51913546C>T , CM000674.2:g.51913546C>T	GRCh38
NC_000012.11:g.52307330C>T , CM000674.1:g.52307330C>T	GRCh37
NC_000012.10:g.50593597C>T	NCBI36
NG_009549.1:g.11129C>T , LRG_543:g.11129C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547400.6:c.355+196C>T	ENSP00000446724.2:n.355+196C>T
ENST00000551576.6:c.314-13C>T	ENSP00000455848.2:n.314-13C>T
ENST00000552678.2:c.314-13C>T	ENSP00000457394.2:n.314-13C>T
ENST00000388922.9:c.314-13C>T MANE Select	ENSP00000373574.4:n.314-13C>T
ENST00000388922.8:c.314-13C>T	ENSP00000373574.4:n.314-13C>T
ENST00000419526.6:c.104-893C>T	ENSP00000392492.2:n.104-893C>T
ENST00000547400.5:c.355+196C>T	ENSP00000446724.1:n.355+196C>T
ENST00000550683.5:c.356-13C>T	ENSP00000447884.1:n.356-13C>T
NM_000020.2:c.314-13C>T , LRG_543t1:c.314-13C>T	NP_000011.2:n.314-13C>T
NM_001077401.1:c.314-13C>T	NP_001070869.1:n.314-13C>T
XM_005269235.2:c.314-13C>T	XP_005269292.1:n.314-13C>T
XM_011539008.1:c.355+196C>T	XP_011537310.1:n.355+196C>T
XM_024449279.1:c.-376-13C>T	XP_024305047.1:n.-376-13C>T
NM_000020.3:c.314-13C>T MANE Select	NP_000011.2:n.314-13C>T
NM_001077401.2:c.314-13C>T	NP_001070869.1:n.314-13C>T