Canonical Allele Identifier: CA2539573527
Gene: GPD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.156578867_156578868insATAATTTATA , CM000664.2:g.156578867_156578868insATAATTTATA GRCh38
NC_000002.11:g.157435379_157435380insATAATTTATA , CM000664.1:g.157435379_157435380insATAATTTATA GRCh37
NC_000002.10:g.157143625_157143626insATAATTTATA NCBI36
NG_016606.1:g.148415_148416insATAATTTATA
NG_016606.2:g.148415_148416insATAATTTATA

Transcript Alleles

HGVS Amino-acid Change
ENST00000438166.7:c.1768-22_1768-21insATAATTTATA MANE Select ENSP00000409708.2:n.1768-22_1768-21insATAATTTATA
ENST00000310454.10:c.1768-22_1768-21insATAATTTATA ENSP00000308610.5:n.1768-22_1768-21insATAATTTATA
ENST00000409125.8:c.1390-22_1390-21insATAATTTATA ENSP00000386484.5:n.1390-22_1390-21insATAATTTATA
ENST00000409674.5:c.1768-22_1768-21insATAATTTATA ENSP00000386425.1:n.1768-22_1768-21insATAATTTATA
ENST00000409861.5:c.1768-22_1768-21insATAATTTATA ENSP00000386626.1:n.1768-22_1768-21insATAATTTATA
ENST00000438166.6:c.1768-22_1768-21insATAATTTATA ENSP00000409708.2:n.1768-22_1768-21insATAATTTATA
ENST00000464846.5:n.122-22_122-21insATAATTTATA
ENST00000540309.5:c.1135-219_1135-218insATAATTTATA ENSP00000440892.1:n.1135-219_1135-218insATAATTTATA
NM_000408.4:c.1768-22_1768-21insATAATTTATA NP_000399.3:n.1768-22_1768-21insATAATTTATA
NM_001083112.2:c.1768-22_1768-21insATAATTTATA NP_001076581.2:n.1768-22_1768-21insATAATTTATA
XM_005246469.1:c.1768-22_1768-21insATAATTTATA XP_005246526.1:n.1768-22_1768-21insATAATTTATA
XM_005246470.3:c.1666-22_1666-21insATAATTTATA XP_005246527.1:n.1666-22_1666-21insATAATTTATA
XM_011510977.1:c.1768-22_1768-21insATAATTTATA XP_011509279.1:n.1768-22_1768-21insATAATTTATA
XM_011510978.1:c.1666-22_1666-21insATAATTTATA XP_011509280.1:n.1666-22_1666-21insATAATTTATA
XM_011510979.1:c.1390-22_1390-21insATAATTTATA XP_011509281.1:n.1390-22_1390-21insATAATTTATA
XM_011510980.1:c.1087-22_1087-21insATAATTTATA XP_011509282.1:n.1087-22_1087-21insATAATTTATA
XM_005246469.2:c.1768-22_1768-21insATAATTTATA XP_005246526.1:n.1768-22_1768-21insATAATTTATA
XM_011510977.2:c.1768-22_1768-21insATAATTTATA XP_011509279.1:n.1768-22_1768-21insATAATTTATA
XM_011510978.2:c.1666-22_1666-21insATAATTTATA XP_011509280.1:n.1666-22_1666-21insATAATTTATA
XM_017003830.1:c.1768-22_1768-21insATAATTTATA XP_016859319.1:n.1768-22_1768-21insATAATTTATA
XM_024452798.1:c.1768-22_1768-21insATAATTTATA XP_024308566.1:n.1768-22_1768-21insATAATTTATA
NM_000408.5:c.1768-22_1768-21insATAATTTATA MANE Select NP_000399.3:n.1768-22_1768-21insATAATTTATA
NM_001083112.3:c.1768-22_1768-21insATAATTTATA NP_001076581.2:n.1768-22_1768-21insATAATTTATA