Canonical Allele Identifier: CA10680863

Gene: ALG14

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.95050081T>G , CM000663.2:g.95050081T>G	GRCh38
NC_000001.10:g.95515637T>G , CM000663.1:g.95515637T>G	GRCh37
NC_000001.9:g.95288225T>G	NCBI36
NG_042044.1:g.27871A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370205.6:c.288+14785A>C MANE Select	ENSP00000359224.4:n.288+14785A>C
ENST00000370205.5:c.288+14785A>C	ENSP00000359224.4:n.288+14785A>C
ENST00000495856.1:n.265-8469A>C
NM_001305242.1:c.289-14199A>C	NP_001292171.1:n.289-14199A>C
NM_144988.3:c.288+14785A>C	NP_659425.1:n.288+14785A>C
NR_131032.1:n.189+22682A>C
XM_005270582.2:c.288+14785A>C	XP_005270639.1:n.288+14785A>C
XM_011540897.1:c.288+14785A>C	XP_011539199.1:n.288+14785A>C
XR_946568.1:n.353+14785A>C
XM_005270582.4:c.288+14785A>C	XP_005270639.1:n.288+14785A>C
XM_011540897.2:c.288+14785A>C	XP_011539199.1:n.288+14785A>C
XR_001737024.1:n.365-8469A>C
XR_001737025.1:n.365-8469A>C
XR_946568.3:n.363+14785A>C
NM_144988.4:c.288+14785A>C MANE Select	NP_659425.1:n.288+14785A>C
NM_001305242.2:c.289-14199A>C	NP_001292171.1:n.289-14199A>C
NR_131032.2:n.189+22682A>C