Canonical Allele Identifier: CA515854635
Gene: GK HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.30742150A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30724033A>G , CM000685.2:g.30724033A>G GRCh38
NC_000023.10:g.30742150A>G , CM000685.1:g.30742150A>G GRCh37
NC_000023.9:g.30652071A>G NCBI36
NG_008178.1:g.75675A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000692461.1:c.1568-68A>G ENSP00000509378.1:n.1568-68A>G
ENST00000427190.6:c.1502-68A>G MANE Select ENSP00000401720.2:n.1502-68A>G
ENST00000479048.6:c.*1205-68A>G ENSP00000420676.1:n.*1205-68A>G
ENST00000378943.7:c.1484-68A>G ENSP00000368226.3:n.1484-68A>G
ENST00000378945.7:c.1484-68A>G ENSP00000368228.3:n.1484-68A>G
ENST00000378946.7:c.1502-68A>G ENSP00000368229.3:n.1502-68A>G
ENST00000427190.5:c.1502-68A>G ENSP00000401720.2:n.1502-68A>G
ENST00000481024.5:c.*1358-68A>G ENSP00000418873.1:n.*1358-68A>G
NM_000167.5:c.1484-68A>G NP_000158.1:n.1484-68A>G
NM_001128127.2:c.1484-68A>G NP_001121599.1:n.1484-68A>G
NM_001205019.1:c.1502-68A>G NP_001191948.1:n.1502-68A>G
NM_203391.3:c.1502-68A>G NP_976325.1:n.1502-68A>G
XM_005274488.3:c.869-68A>G XP_005274545.1:n.869-68A>G
XM_006724483.2:c.1568-68A>G XP_006724546.1:n.1568-68A>G
XM_006724484.2:c.1568-68A>G XP_006724547.1:n.1568-68A>G
XM_006724485.2:c.887-68A>G XP_006724548.1:n.887-68A>G
XM_006724486.2:c.887-68A>G XP_006724549.1:n.887-68A>G
XM_011545491.1:c.1586-68A>G XP_011543793.1:n.1586-68A>G
XM_011545492.1:c.1586-68A>G XP_011543794.1:n.1586-68A>G
XM_011545493.1:c.887-68A>G XP_011543795.1:n.887-68A>G
XM_011545494.1:c.887-68A>G XP_011543796.1:n.887-68A>G
XM_005274488.4:c.869-68A>G XP_005274545.1:n.869-68A>G
XM_006724486.3:c.887-68A>G XP_006724549.1:n.887-68A>G
XM_011545491.2:c.1586-68A>G XP_011543793.1:n.1586-68A>G
XM_011545493.2:c.887-68A>G XP_011543795.1:n.887-68A>G
XM_011545494.2:c.887-68A>G XP_011543796.1:n.887-68A>G
XM_017029409.1:c.887-68A>G XP_016884898.1:n.887-68A>G
XM_017029410.1:c.887-68A>G XP_016884899.1:n.887-68A>G
XM_017029411.1:c.869-68A>G XP_016884900.1:n.869-68A>G
XM_017029412.2:c.869-68A>G XP_016884901.1:n.869-68A>G
NM_000167.6:c.1484-68A>G NP_000158.1:n.1484-68A>G
NM_001128127.3:c.1484-68A>G NP_001121599.1:n.1484-68A>G
NM_001205019.2:c.1502-68A>G MANE Select NP_001191948.1:n.1502-68A>G
NM_203391.4:c.1502-68A>G NP_976325.1:n.1502-68A>G
NM_001399987.1:c.1568-68A>G NP_001386916.1:n.1568-68A>G
NR_174369.1:n.1782-68A>G
NR_174370.1:n.1510-68A>G
NR_174371.1:n.1436-68A>G
NR_174372.1:n.1418-68A>G
NR_174373.1:n.1492-68A>G
NR_174374.1:n.1436-68A>G
NR_174375.1:n.1418-68A>G