Canonical Allele Identifier: CA2422182004

Gene: GK

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.30724069_30724070delinsCG , CM000685.2:g.30724069_30724070delinsCG	GRCh38
NC_000023.10:g.30742186_30742187delinsCG , CM000685.1:g.30742186_30742187delinsCG	GRCh37
NC_000023.9:g.30652107_30652108delinsCG	NCBI36
NG_008178.1:g.75711_75712delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000692461.1:c.1568-32_1568-31delinsCG	ENSP00000509378.1:n.1568-32_1568-31delinsCG
ENST00000427190.6:c.1502-32_1502-31delinsCG MANE Select	ENSP00000401720.2:n.1502-32_1502-31delinsCG
ENST00000479048.6:c.*1205-32_*1205-31delinsCG	ENSP00000420676.1:n.*1205-32_*1205-31delinsCG
ENST00000378943.7:c.1484-32_1484-31delinsCG	ENSP00000368226.3:n.1484-32_1484-31delinsCG
ENST00000378945.7:c.1484-32_1484-31delinsCG	ENSP00000368228.3:n.1484-32_1484-31delinsCG
ENST00000378946.7:c.1502-32_1502-31delinsCG	ENSP00000368229.3:n.1502-32_1502-31delinsCG
ENST00000427190.5:c.1502-32_1502-31delinsCG	ENSP00000401720.2:n.1502-32_1502-31delinsCG
ENST00000481024.5:c.*1358-32_*1358-31delinsCG	ENSP00000418873.1:n.*1358-32_*1358-31delinsCG
NM_000167.5:c.1484-32_1484-31delinsCG	NP_000158.1:n.1484-32_1484-31delinsCG
NM_001128127.2:c.1484-32_1484-31delinsCG	NP_001121599.1:n.1484-32_1484-31delinsCG
NM_001205019.1:c.1502-32_1502-31delinsCG	NP_001191948.1:n.1502-32_1502-31delinsCG
NM_203391.3:c.1502-32_1502-31delinsCG	NP_976325.1:n.1502-32_1502-31delinsCG
XM_005274488.3:c.869-32_869-31delinsCG	XP_005274545.1:n.869-32_869-31delinsCG
XM_006724483.2:c.1568-32_1568-31delinsCG	XP_006724546.1:n.1568-32_1568-31delinsCG
XM_006724484.2:c.1568-32_1568-31delinsCG	XP_006724547.1:n.1568-32_1568-31delinsCG
XM_006724485.2:c.887-32_887-31delinsCG	XP_006724548.1:n.887-32_887-31delinsCG
XM_006724486.2:c.887-32_887-31delinsCG	XP_006724549.1:n.887-32_887-31delinsCG
XM_011545491.1:c.1586-32_1586-31delinsCG	XP_011543793.1:n.1586-32_1586-31delinsCG
XM_011545492.1:c.1586-32_1586-31delinsCG	XP_011543794.1:n.1586-32_1586-31delinsCG
XM_011545493.1:c.887-32_887-31delinsCG	XP_011543795.1:n.887-32_887-31delinsCG
XM_011545494.1:c.887-32_887-31delinsCG	XP_011543796.1:n.887-32_887-31delinsCG
XM_005274488.4:c.869-32_869-31delinsCG	XP_005274545.1:n.869-32_869-31delinsCG
XM_006724486.3:c.887-32_887-31delinsCG	XP_006724549.1:n.887-32_887-31delinsCG
XM_011545491.2:c.1586-32_1586-31delinsCG	XP_011543793.1:n.1586-32_1586-31delinsCG
XM_011545493.2:c.887-32_887-31delinsCG	XP_011543795.1:n.887-32_887-31delinsCG
XM_011545494.2:c.887-32_887-31delinsCG	XP_011543796.1:n.887-32_887-31delinsCG
XM_017029409.1:c.887-32_887-31delinsCG	XP_016884898.1:n.887-32_887-31delinsCG
XM_017029410.1:c.887-32_887-31delinsCG	XP_016884899.1:n.887-32_887-31delinsCG
XM_017029411.1:c.869-32_869-31delinsCG	XP_016884900.1:n.869-32_869-31delinsCG
XM_017029412.2:c.869-32_869-31delinsCG	XP_016884901.1:n.869-32_869-31delinsCG
NM_000167.6:c.1484-32_1484-31delinsCG	NP_000158.1:n.1484-32_1484-31delinsCG
NM_001128127.3:c.1484-32_1484-31delinsCG	NP_001121599.1:n.1484-32_1484-31delinsCG
NM_001205019.2:c.1502-32_1502-31delinsCG MANE Select	NP_001191948.1:n.1502-32_1502-31delinsCG
NM_203391.4:c.1502-32_1502-31delinsCG	NP_976325.1:n.1502-32_1502-31delinsCG
NM_001399987.1:c.1568-32_1568-31delinsCG	NP_001386916.1:n.1568-32_1568-31delinsCG
NR_174369.1:n.1782-32_1782-31delinsCG
NR_174370.1:n.1510-32_1510-31delinsCG
NR_174371.1:n.1436-32_1436-31delinsCG
NR_174372.1:n.1418-32_1418-31delinsCG
NR_174373.1:n.1492-32_1492-31delinsCG
NR_174374.1:n.1436-32_1436-31delinsCG
NR_174375.1:n.1418-32_1418-31delinsCG