Canonical Allele Identifier: CA626016678
Gene: KRT16 HGNC NCBI

Linked Data

dbSNP Id: rs1165908478
gnomAD v2: 17-39768949-G-A
MyVariant Identifiers: chr17:g.39768949G>A (hg19) chr17:g.41612697G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612697G>A , CM000679.2:g.41612697G>A GRCh38
NC_000017.10:g.39768949G>A , CM000679.1:g.39768949G>A GRCh37
NC_000017.9:g.37022475G>A NCBI36
NG_008301.1:g.5131C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.-9C>T MANE Select ENSP00000301653.3:n.-9C>T
ENST00000301653.8:c.-9C>T ENSP00000301653.3:n.-9C>T
ENST00000588319.1:n.69C>T
ENST00000590990.1:c.-9C>T ENSP00000467105.1:n.-9C>T
ENST00000593067.1:c.-313+93C>T ENSP00000467124.1:n.-313+93C>T
NM_005557.3:c.-9C>T NP_005548.2:n.-9C>T
NM_005557.4:c.-9C>T MANE Select NP_005548.2:n.-9C>T
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