Canonical Allele Identifier: CA8563387
Gene: KRT16 HGNC NCBI

Linked Data

dbSNP Id: rs768296966
ExAC: 17:39768964 A / T
gnomAD v2: 17-39768964-A-T
gnomAD v4: 17-41612712-A-T
MyVariant Identifiers: chr17:g.39768964A>T (hg19) chr17:g.41612712A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612712A>T , CM000679.2:g.41612712A>T GRCh38
NC_000017.10:g.39768964A>T , CM000679.1:g.39768964A>T GRCh37
NC_000017.9:g.37022490A>T NCBI36
NG_008301.1:g.5116T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.-24T>A MANE Select ENSP00000301653.3:n.-24T>A
ENST00000301653.8:c.-24T>A ENSP00000301653.3:n.-24T>A
ENST00000588319.1:n.54T>A
ENST00000590990.1:c.-24T>A ENSP00000467105.1:n.-24T>A
ENST00000593067.1:c.-313+78T>A ENSP00000467124.1:n.-313+78T>A
NM_005557.3:c.-24T>A NP_005548.2:n.-24T>A
NM_005557.4:c.-24T>A MANE Select NP_005548.2:n.-24T>A
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