Canonical Allele Identifier: CA2259745933
Gene: KRT12 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40867055_40867056delinsTC , CM000679.2:g.40867055_40867056delinsTC GRCh38
NC_000017.10:g.39023307_39023308delinsTC , CM000679.1:g.39023307_39023308delinsTC GRCh37
NC_000017.9:g.36276833_36276834delinsTC NCBI36
NG_008077.1:g.5155_5156delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000251643.5:c.131_132delinsGA MANE Select ENSP00000251643.4:p.Gly44=
ENST00000647902.1:c.131_132delinsGA ENSP00000497770.1:p.Gly44=
ENST00000251643.4:c.131_132delinsGA ENSP00000251643.4:p.Gly44=
NM_000223.3:c.131_132delinsGA NP_000214.1:p.Gly44=
XR_934754.1:n.1500+16195_1500+16196delinsTC
XR_934754.2:n.2008+16195_2008+16196delinsTC
NM_000223.4:c.131_132delinsGA MANE Select NP_000214.1:p.Gly44=
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