Canonical Allele Identifier: CA2561782829

Gene: ALG14 ALG14-AS1

Linked Data

• ClinVar Variation Id: 2119320
• ClinVar RCV Id: RCV003054600

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.95065032A>G , CM000663.2:g.95065032A>G	GRCh38
NC_000001.10:g.95530588A>G , CM000663.1:g.95530588A>G	GRCh37
NC_000001.9:g.95303176A>G	NCBI36
NG_042044.1:g.12920T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370205.6:c.137-15T>C (ALG14) MANE Select	ENSP00000359224.4:n.137-15T>C
ENST00000370205.5:c.137-15T>C (ALG14)	ENSP00000359224.4:n.137-15T>C
ENST00000495856.1:n.113-15T>C (ALG14)
NM_001305242.1:c.137-15T>C (ALG14)	NP_001292171.1:n.137-15T>C
NM_144988.3:c.137-15T>C (ALG14)	NP_659425.1:n.137-15T>C
NR_131032.1:n.189+7731T>C (ALG14)
NR_132786.1:n.595-2012A>G (ALG14-AS1)
XM_005270582.2:c.137-15T>C (ALG14)	XP_005270639.1:n.137-15T>C
XM_011540897.1:c.137-15T>C (ALG14)	XP_011539199.1:n.137-15T>C
XR_946568.1:n.202-15T>C (ALG14)
XM_005270582.4:c.137-15T>C (ALG14)	XP_005270639.1:n.137-15T>C
XM_011540897.2:c.137-15T>C (ALG14)	XP_011539199.1:n.137-15T>C
XR_001737024.1:n.213-15T>C (ALG14)
XR_001737025.1:n.213-15T>C (ALG14)
XR_946568.3:n.212-15T>C (ALG14)
NM_144988.4:c.137-15T>C (ALG14) MANE Select	NP_659425.1:n.137-15T>C
NM_001305242.2:c.137-15T>C (ALG14)	NP_001292171.1:n.137-15T>C
NR_131032.2:n.189+7731T>C (ALG14)