Canonical Allele Identifier: CA399496927
Gene: KRT16 HGNC NCBI

Linked Data

gnomAD v4: 17-41612619-T-A
MyVariant Identifiers: chr17:g.39768871T>A (hg19) chr17:g.41612619T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612619T>A , CM000679.2:g.41612619T>A GRCh38
NC_000017.10:g.39768871T>A , CM000679.1:g.39768871T>A GRCh37
NC_000017.9:g.37022397T>A NCBI36
NG_008301.1:g.5209A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.70A>T MANE Select ENSP00000301653.3:p.Ile24Phe
ENST00000301653.8:c.70A>T ENSP00000301653.3:p.Ile24Phe
ENST00000588319.1:n.147A>T
ENST00000590990.1:c.70A>T ENSP00000467105.1:p.Ile24Phe
ENST00000593067.1:c.-313+171A>T ENSP00000467124.1:n.-313+171A>T
NM_005557.3:c.70A>T NP_005548.2:p.Ile24Phe
NM_005557.4:c.70A>T MANE Select NP_005548.2:p.Ile24Phe
Search 100 bp 5'
Search 100 bp 3'