Canonical Allele Identifier: CA2646882463
Gene: AKNAD1 HGNC NCBI
GPSM2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.108876912C>T , CM000663.2:g.108876912C>T GRCh38
NC_000001.10:g.109419534C>T , CM000663.1:g.109419534C>T GRCh37
NC_000001.9:g.109221057C>T NCBI36
NG_028108.1:g.4932C>T
NG_028108.2:g.6563C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000357393.6:c.1-27336G>A (AKNAD1) ENSP00000349968.6:n.1-27336G>A
ENST00000357393.5:c.115-27336G>A ENSP00000349968.5:n.115-27336G>A
ENST00000406462.6:c.-565C>T (GPSM2) ENSP00000385510.1:n.-565C>T
XM_005270787.2:c.-333C>T (GPSM2) XP_005270844.1:n.-333C>T
XM_006710589.1:c.-318C>T (GPSM2) XP_006710652.1:n.-318C>T
XM_011541301.1:c.-565C>T (GPSM2) XP_011539603.1:n.-565C>T
XM_011541303.1:c.-565C>T (GPSM2) XP_011539605.1:n.-565C>T
XM_006710589.3:c.-318C>T (GPSM2) XP_006710652.1:n.-318C>T
XM_011541301.2:c.-565C>T (GPSM2) XP_011539603.1:n.-565C>T
XM_011541302.3:c.-809C>T (GPSM2) XP_011539604.1:n.-809C>T
XM_011541303.3:c.-565C>T (GPSM2) XP_011539605.1:n.-565C>T
XM_017001097.2:c.-715C>T (GPSM2) XP_016856586.1:n.-715C>T
XM_017001098.2:c.-483C>T (GPSM2) XP_016856587.1:n.-483C>T