Canonical Allele Identifier: CA1300570972
Gene: GPD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.156579222_156579223delinsTG , CM000664.2:g.156579222_156579223delinsTG GRCh38
NC_000002.11:g.157435734_157435735delinsTG , CM000664.1:g.157435734_157435735delinsTG GRCh37
NC_000002.10:g.157143980_157143981delinsTG NCBI36
NG_016606.1:g.148770_148771delinsTG
NG_016606.2:g.148770_148771delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000438166.7:c.1959+58_1959+59delinsTG MANE Select ENSP00000409708.2:n.1959+58_1959+59delinsTG
ENST00000310454.10:c.1959+58_1959+59delinsTG ENSP00000308610.5:n.1959+58_1959+59delinsTG
ENST00000409125.8:c.1581+58_1581+59delinsTG ENSP00000386484.5:n.1581+58_1581+59delinsTG
ENST00000409674.5:c.1959+58_1959+59delinsTG ENSP00000386425.1:n.1959+58_1959+59delinsTG
ENST00000409861.5:c.1959+58_1959+59delinsTG ENSP00000386626.1:n.1959+58_1959+59delinsTG
ENST00000438166.6:c.1959+58_1959+59delinsTG ENSP00000409708.2:n.1959+58_1959+59delinsTG
ENST00000464846.5:n.397+58_397+59delinsTG
ENST00000492005.1:n.82+58_82+59delinsTG
ENST00000540309.5:c.*73+58_*73+59delinsTG ENSP00000440892.1:n.*73+58_*73+59delinsTG
NM_000408.4:c.1959+58_1959+59delinsTG NP_000399.3:n.1959+58_1959+59delinsTG
NM_001083112.2:c.1959+58_1959+59delinsTG NP_001076581.2:n.1959+58_1959+59delinsTG
XM_005246469.1:c.1959+58_1959+59delinsTG XP_005246526.1:n.1959+58_1959+59delinsTG
XM_005246470.3:c.1857+58_1857+59delinsTG XP_005246527.1:n.1857+58_1857+59delinsTG
XM_011510977.1:c.1959+58_1959+59delinsTG XP_011509279.1:n.1959+58_1959+59delinsTG
XM_011510978.1:c.1857+58_1857+59delinsTG XP_011509280.1:n.1857+58_1857+59delinsTG
XM_011510979.1:c.1581+58_1581+59delinsTG XP_011509281.1:n.1581+58_1581+59delinsTG
XM_011510980.1:c.1278+58_1278+59delinsTG XP_011509282.1:n.1278+58_1278+59delinsTG
XM_005246469.2:c.1959+58_1959+59delinsTG XP_005246526.1:n.1959+58_1959+59delinsTG
XM_011510977.2:c.1959+58_1959+59delinsTG XP_011509279.1:n.1959+58_1959+59delinsTG
XM_011510978.2:c.1857+58_1857+59delinsTG XP_011509280.1:n.1857+58_1857+59delinsTG
XM_017003830.1:c.1959+58_1959+59delinsTG XP_016859319.1:n.1959+58_1959+59delinsTG
XM_024452798.1:c.1959+58_1959+59delinsTG XP_024308566.1:n.1959+58_1959+59delinsTG
NM_000408.5:c.1959+58_1959+59delinsTG MANE Select NP_000399.3:n.1959+58_1959+59delinsTG
NM_001083112.3:c.1959+58_1959+59delinsTG NP_001076581.2:n.1959+58_1959+59delinsTG