Canonical Allele Identifier: CA1116710

Gene: S100A14

Linked Data - Expert Curation

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153615864C>T , CM000663.2:g.153615864C>T	GRCh38
NC_000001.10:g.153588340C>T , CM000663.1:g.153588340C>T	GRCh37
NC_000001.9:g.151854964C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344616.4:c.-6G>A MANE Select	ENSP00000340463.2:n.-6G>A
ENST00000344616.3:c.-6G>A	ENSP00000340463.2:n.-6G>A
ENST00000368700.7:n.101+4G>A
ENST00000368701.5:c.-6G>A	ENSP00000357690.1:n.-6G>A
ENST00000368702.5:c.-6G>A	ENSP00000357691.1:n.-6G>A
ENST00000469571.1:n.148G>A
ENST00000476873.5:c.-6G>A	ENSP00000420296.1:n.-6G>A
NM_020672.2:c.-6G>A	NP_065723.1:n.-6G>A
XM_005245362.1:c.-6G>A	XP_005245419.1:n.-6G>A
XM_017001875.1:c.-6G>A	XP_016857364.1:n.-6G>A
NM_020672.3:c.-6G>A MANE Select	NP_065723.1:n.-6G>A