Canonical Allele Identifier: CA128354241
Community Standard Title: NM_006083.4(IK):c.16+122A>G
Gene: IK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140648046A>G , CM000667.2:g.140648046A>G GRCh38
NC_000005.9:g.140027631A>G , CM000667.1:g.140027631A>G GRCh37
NC_000005.8:g.140007815A>G NCBI36
NG_021417.1:g.4740T>C

Transcript Alleles

HGVS Amino-acid Change
NM_006083.4:c.16+122A>G MANE Select NP_006074.2:n.16+122A>G
ENST00000417647.7:c.16+122A>G MANE Select ENSP00000396301.2:n.16+122A>G
NM_006083.3:c.16+122A>G NP_006074.2:n.16+122A>G
ENST00000417647.6:c.16+122A>G ENSP00000396301.2:n.16+122A>G
ENST00000503332.5:c.16+122A>G ENSP00000421930.1:n.16+122A>G
ENST00000507593.5:c.16+122A>G ENSP00000424622.1:n.16+122A>G
ENST00000508301.5:c.16+122A>G ENSP00000422641.1:n.16+122A>G
ENST00000513256.5:c.5-425A>G ENSP00000425564.1:n.5-425A>G
ENST00000523672.1:n.80+39A>G
ENST00000620556.4:c.16+122A>G ENSP00000480993.1:n.16+122A>G
XR_002956156.1:n.107+122A>G