Canonical Allele Identifier: CA399497429
Gene: KRT16 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39768919A>G (hg19) chr17:g.41612667A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612667A>G , CM000679.2:g.41612667A>G GRCh38
NC_000017.10:g.39768919A>G , CM000679.1:g.39768919A>G GRCh37
NC_000017.9:g.37022445A>G NCBI36
NG_008301.1:g.5161T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.22T>C MANE Select ENSP00000301653.3:p.Phe8Leu
ENST00000301653.8:c.22T>C ENSP00000301653.3:p.Phe8Leu
ENST00000588319.1:n.99T>C
ENST00000590990.1:c.22T>C ENSP00000467105.1:p.Phe8Leu
ENST00000593067.1:c.-313+123T>C ENSP00000467124.1:n.-313+123T>C
NM_005557.3:c.22T>C NP_005548.2:p.Phe8Leu
NM_005557.4:c.22T>C MANE Select NP_005548.2:p.Phe8Leu
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