Canonical Allele Identifier: CA399495059
Gene: KRT16 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39768613C>T (hg19) chr17:g.41612361C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612361C>T , CM000679.2:g.41612361C>T GRCh38
NC_000017.10:g.39768613C>T , CM000679.1:g.39768613C>T GRCh37
NC_000017.9:g.37022139C>T NCBI36
NG_008301.1:g.5467G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.328G>A MANE Select ENSP00000301653.3:p.Asp110Asn
ENST00000301653.8:c.328G>A ENSP00000301653.3:p.Asp110Asn
ENST00000588319.1:n.405G>A
ENST00000593067.1:c.-312-75G>A ENSP00000467124.1:n.-312-75G>A
NM_005557.3:c.328G>A NP_005548.2:p.Asp110Asn
NM_005557.4:c.328G>A MANE Select NP_005548.2:p.Asp110Asn
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