Canonical Allele Identifier: CA2036500984
Gene: KRT6B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52451695_52451696delinsAG , CM000674.2:g.52451695_52451696delinsAG GRCh38
NC_000012.11:g.52845479_52845480delinsAG , CM000674.1:g.52845479_52845480delinsAG GRCh37
NC_000012.10:g.51131746_51131747delinsAG NCBI36
NG_008299.1:g.5431_5432delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000252252.4:c.383_384delinsCT MANE Select ENSP00000252252.3:p.Pro128=
ENST00000252252.3:c.383_384delinsCT ENSP00000252252.3:p.Pro128=
NM_005555.3:c.383_384delinsCT NP_005546.2:p.Pro128=
NM_005555.4:c.383_384delinsCT MANE Select NP_005546.2:p.Pro128=
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