Canonical Allele Identifier: CA2259745964
Gene: KRT12 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40867122_40867123delinsGA , CM000679.2:g.40867122_40867123delinsGA GRCh38
NC_000017.10:g.39023374_39023375delinsGA , CM000679.1:g.39023374_39023375delinsGA GRCh37
NC_000017.9:g.36276900_36276901delinsGA NCBI36
NG_008077.1:g.5088_5089delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000251643.5:c.64_65delinsTC MANE Select ENSP00000251643.4:p.Ser22=
ENST00000647902.1:c.64_65delinsTC ENSP00000497770.1:p.Ser22=
ENST00000251643.4:c.64_65delinsTC ENSP00000251643.4:p.Ser22=
NM_000223.3:c.64_65delinsTC NP_000214.1:p.Ser22=
XR_934754.1:n.1500+16262_1500+16263delinsGA
XR_934754.2:n.2008+16262_2008+16263delinsGA
NM_000223.4:c.64_65delinsTC MANE Select NP_000214.1:p.Ser22=
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