Canonical Allele Identifier: CA874575900

Gene: GK

Linked Data

• dbSNP Id: rs1466240225
• gnomAD v3: X-30724005-A-AATTTGTCAAGAATGTTGAGTG
• gnomAD v4: X-30724005-A-AATTTGTCAAGAATGTTGAGTG
• MyVariant Identifiers: chrX:g.30742122_30742123insATTTGTCAAGAATGTTGAGTG (hg19) ; chrX:g.30724005_30724006insATTTGTCAAGAATGTTGAGTG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.30724008_30724028dup , CM000685.2:g.30724008_30724028dup	GRCh38
NC_000023.10:g.30742125_30742145dup , CM000685.1:g.30742125_30742145dup	GRCh37
NC_000023.9:g.30652046_30652066dup	NCBI36
NG_008178.1:g.75650_75670dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000692461.1:c.1568-93_1568-73dup	ENSP00000509378.1:n.1568-93_1568-73dup
ENST00000427190.6:c.1502-93_1502-73dup MANE Select	ENSP00000401720.2:n.1502-93_1502-73dup
ENST00000479048.6:c.*1205-93_*1205-73dup	ENSP00000420676.1:n.*1205-93_*1205-73dup
ENST00000378943.7:c.1484-93_1484-73dup	ENSP00000368226.3:n.1484-93_1484-73dup
ENST00000378945.7:c.1484-93_1484-73dup	ENSP00000368228.3:n.1484-93_1484-73dup
ENST00000378946.7:c.1502-93_1502-73dup	ENSP00000368229.3:n.1502-93_1502-73dup
ENST00000427190.5:c.1502-93_1502-73dup	ENSP00000401720.2:n.1502-93_1502-73dup
ENST00000481024.5:c.*1358-93_*1358-73dup	ENSP00000418873.1:n.*1358-93_*1358-73dup
NM_000167.5:c.1484-93_1484-73dup	NP_000158.1:n.1484-93_1484-73dup
NM_001128127.2:c.1484-93_1484-73dup	NP_001121599.1:n.1484-93_1484-73dup
NM_001205019.1:c.1502-93_1502-73dup	NP_001191948.1:n.1502-93_1502-73dup
NM_203391.3:c.1502-93_1502-73dup	NP_976325.1:n.1502-93_1502-73dup
XM_005274488.3:c.869-93_869-73dup	XP_005274545.1:n.869-93_869-73dup
XM_006724483.2:c.1568-93_1568-73dup	XP_006724546.1:n.1568-93_1568-73dup
XM_006724484.2:c.1568-93_1568-73dup	XP_006724547.1:n.1568-93_1568-73dup
XM_006724485.2:c.887-93_887-73dup	XP_006724548.1:n.887-93_887-73dup
XM_006724486.2:c.887-93_887-73dup	XP_006724549.1:n.887-93_887-73dup
XM_011545491.1:c.1586-93_1586-73dup	XP_011543793.1:n.1586-93_1586-73dup
XM_011545492.1:c.1586-93_1586-73dup	XP_011543794.1:n.1586-93_1586-73dup
XM_011545493.1:c.887-93_887-73dup	XP_011543795.1:n.887-93_887-73dup
XM_011545494.1:c.887-93_887-73dup	XP_011543796.1:n.887-93_887-73dup
XM_005274488.4:c.869-93_869-73dup	XP_005274545.1:n.869-93_869-73dup
XM_006724486.3:c.887-93_887-73dup	XP_006724549.1:n.887-93_887-73dup
XM_011545491.2:c.1586-93_1586-73dup	XP_011543793.1:n.1586-93_1586-73dup
XM_011545493.2:c.887-93_887-73dup	XP_011543795.1:n.887-93_887-73dup
XM_011545494.2:c.887-93_887-73dup	XP_011543796.1:n.887-93_887-73dup
XM_017029409.1:c.887-93_887-73dup	XP_016884898.1:n.887-93_887-73dup
XM_017029410.1:c.887-93_887-73dup	XP_016884899.1:n.887-93_887-73dup
XM_017029411.1:c.869-93_869-73dup	XP_016884900.1:n.869-93_869-73dup
XM_017029412.2:c.869-93_869-73dup	XP_016884901.1:n.869-93_869-73dup
NM_000167.6:c.1484-93_1484-73dup	NP_000158.1:n.1484-93_1484-73dup
NM_001128127.3:c.1484-93_1484-73dup	NP_001121599.1:n.1484-93_1484-73dup
NM_001205019.2:c.1502-93_1502-73dup MANE Select	NP_001191948.1:n.1502-93_1502-73dup
NM_203391.4:c.1502-93_1502-73dup	NP_976325.1:n.1502-93_1502-73dup
NM_001399987.1:c.1568-93_1568-73dup	NP_001386916.1:n.1568-93_1568-73dup
NR_174369.1:n.1782-93_1782-73dup
NR_174370.1:n.1510-93_1510-73dup
NR_174371.1:n.1436-93_1436-73dup
NR_174372.1:n.1418-93_1418-73dup
NR_174373.1:n.1492-93_1492-73dup
NR_174374.1:n.1436-93_1436-73dup
NR_174375.1:n.1418-93_1418-73dup