Canonical Allele Identifier: CA2260099715
Gene: KRT16 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612348A= , CM000679.2:g.41612348A= GRCh38
NC_000017.10:g.39768600A= , CM000679.1:g.39768600A= GRCh37
NC_000017.9:g.37022126A= NCBI36
NG_008301.1:g.5480T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.341T= MANE Select ENSP00000301653.3:p.Val114=
ENST00000301653.8:c.341T= ENSP00000301653.3:p.Val114=
ENST00000588319.1:n.418T=
ENST00000593067.1:c.-312-62T= ENSP00000467124.1:n.-312-62T=
NM_005557.3:c.341T= NP_005548.2:p.Val114=
NM_005557.4:c.341T= MANE Select NP_005548.2:p.Val114=
Search 100 bp 5'
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