Canonical Allele Identifier: CA2499226609
Community Standard Title: NM_001205019.2(GK):c.784-79_784-78insTAAA
Gene: GK HGNC NCBI
GK-AS1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30700759_30700760insTAAA , CM000685.2:g.30700759_30700760insTAAA GRCh38
NC_000023.10:g.30718876_30718877insTAAA , CM000685.1:g.30718876_30718877insTAAA GRCh37
NC_000023.9:g.30628797_30628798insTAAA NCBI36
NG_008178.1:g.52401_52402insTAAA

Transcript Alleles

HGVS Amino-acid Change
NM_001205019.2:c.784-79_784-78insTAAA (GK) MANE Select NP_001191948.1:n.784-79_784-78insTAAA
ENST00000427190.6:c.784-79_784-78insTAAA (GK) MANE Select ENSP00000401720.2:n.784-79_784-78insTAAA
NM_000167.5:c.766-79_766-78insTAAA (GK) NP_000158.1:n.766-79_766-78insTAAA
NM_000167.6:c.766-79_766-78insTAAA (GK) NP_000158.1:n.766-79_766-78insTAAA
NM_001128127.2:c.766-79_766-78insTAAA (GK) NP_001121599.1:n.766-79_766-78insTAAA
NM_001128127.3:c.766-79_766-78insTAAA (GK) NP_001121599.1:n.766-79_766-78insTAAA
NM_001205019.1:c.784-79_784-78insTAAA (GK) NP_001191948.1:n.784-79_784-78insTAAA
NM_001399987.1:c.850-79_850-78insTAAA (GK) NP_001386916.1:n.850-79_850-78insTAAA
NM_203391.3:c.784-79_784-78insTAAA (GK) NP_976325.1:n.784-79_784-78insTAAA
NM_203391.4:c.784-79_784-78insTAAA (GK) NP_976325.1:n.784-79_784-78insTAAA
NR_046603.1:n.17342_17343insTATT (GK-AS1)
NR_174369.1:n.1064-79_1064-78insTAAA (GK)
NR_174370.1:n.792-79_792-78insTAAA (GK)
NR_174371.1:n.718-79_718-78insTAAA (GK)
NR_174372.1:n.700-79_700-78insTAAA (GK)
NR_174373.1:n.774-79_774-78insTAAA (GK)
NR_174374.1:n.718-79_718-78insTAAA (GK)
NR_174375.1:n.700-79_700-78insTAAA (GK)
ENST00000378943.7:c.766-79_766-78insTAAA (GK) ENSP00000368226.3:n.766-79_766-78insTAAA
ENST00000378945.7:c.766-79_766-78insTAAA (GK) ENSP00000368228.3:n.766-79_766-78insTAAA
ENST00000378946.7:c.784-79_784-78insTAAA (GK) ENSP00000368229.3:n.784-79_784-78insTAAA
ENST00000427190.5:c.784-79_784-78insTAAA (GK) ENSP00000401720.2:n.784-79_784-78insTAAA
ENST00000479048.6:c.*487-79_*487-78insTAAA (GK) ENSP00000420676.1:n.*487-79_*487-78insTAAA
ENST00000481024.5:c.*640-79_*640-78insTAAA (GK) ENSP00000418873.1:n.*640-79_*640-78insTAAA
ENST00000488296.1:c.586-79_586-78insTAAA (GK) ENSP00000419771.1:n.586-79_586-78insTAAA
ENST00000692461.1:c.850-79_850-78insTAAA (GK) ENSP00000509378.1:n.850-79_850-78insTAAA
XM_005274488.3:c.151-79_151-78insTAAA (GK) XP_005274545.1:n.151-79_151-78insTAAA
XM_005274488.4:c.151-79_151-78insTAAA (GK) XP_005274545.1:n.151-79_151-78insTAAA
XM_006724483.2:c.850-79_850-78insTAAA (GK) XP_006724546.1:n.850-79_850-78insTAAA
XM_006724484.2:c.850-79_850-78insTAAA (GK) XP_006724547.1:n.850-79_850-78insTAAA
XM_006724485.2:c.169-79_169-78insTAAA (GK) XP_006724548.1:n.169-79_169-78insTAAA
XM_006724486.2:c.169-79_169-78insTAAA (GK) XP_006724549.1:n.169-79_169-78insTAAA
XM_006724486.3:c.169-79_169-78insTAAA (GK) XP_006724549.1:n.169-79_169-78insTAAA
XM_011545491.1:c.868-79_868-78insTAAA (GK) XP_011543793.1:n.868-79_868-78insTAAA
XM_011545491.2:c.868-79_868-78insTAAA (GK) XP_011543793.1:n.868-79_868-78insTAAA
XM_011545492.1:c.868-79_868-78insTAAA (GK) XP_011543794.1:n.868-79_868-78insTAAA
XM_011545493.1:c.169-79_169-78insTAAA (GK) XP_011543795.1:n.169-79_169-78insTAAA
XM_011545493.2:c.169-79_169-78insTAAA (GK) XP_011543795.1:n.169-79_169-78insTAAA
XM_011545494.1:c.169-79_169-78insTAAA (GK) XP_011543796.1:n.169-79_169-78insTAAA
XM_011545494.2:c.169-79_169-78insTAAA (GK) XP_011543796.1:n.169-79_169-78insTAAA
XM_017029409.1:c.169-79_169-78insTAAA (GK) XP_016884898.1:n.169-79_169-78insTAAA
XM_017029410.1:c.169-79_169-78insTAAA (GK) XP_016884899.1:n.169-79_169-78insTAAA
XM_017029411.1:c.151-79_151-78insTAAA (GK) XP_016884900.1:n.151-79_151-78insTAAA
XM_017029412.2:c.151-79_151-78insTAAA (GK) XP_016884901.1:n.151-79_151-78insTAAA
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