Canonical Allele Identifier: CA399494668
Gene: KRT16 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39768540T>A (hg19) chr17:g.41612288T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612288T>A , CM000679.2:g.41612288T>A GRCh38
NC_000017.10:g.39768540T>A , CM000679.1:g.39768540T>A GRCh37
NC_000017.9:g.37022066T>A NCBI36
NG_008301.1:g.5540A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.401A>T MANE Select ENSP00000301653.3:p.Lys134Met
ENST00000301653.8:c.401A>T ENSP00000301653.3:p.Lys134Met
ENST00000588319.1:n.478A>T
ENST00000593067.1:c.-312-2A>T ENSP00000467124.1:n.-312-2A>T
NM_005557.3:c.401A>T NP_005548.2:p.Lys134Met
NM_005557.4:c.401A>T MANE Select NP_005548.2:p.Lys134Met
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