Canonical Allele Identifier: CA2260099617
Gene: KRT16 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612162_41612170delinsTTCCTCAGG , CM000679.2:g.41612162_41612170delinsTTCCTCAGG GRCh38
NC_000017.10:g.39768414_39768422delinsTTCCTCAGG , CM000679.1:g.39768414_39768422delinsTTCCTCAGG GRCh37
NC_000017.9:g.37021940_37021948delinsTTCCTCAGG NCBI36
NG_008301.1:g.5658_5666delinsCCTGAGGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.519_527delinsCCTGAGGAA MANE Select ENSP00000301653.3:p.Asp173=
ENST00000301653.8:c.519_527delinsCCTGAGGAA ENSP00000301653.3:p.Asp173=
ENST00000588319.1:n.596_604delinsCCTGAGGAA
ENST00000593067.1:c.-196_-188delinsCCTGAGGAA ENSP00000467124.1:n.-196_-188delinsCCTGAGGAA
NM_005557.3:c.519_527delinsCCTGAGGAA NP_005548.2:p.Asp173=
NM_005557.4:c.519_527delinsCCTGAGGAA MANE Select NP_005548.2:p.Asp173=
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