Canonical Allele Identifier: CA2260099944
Gene: KRT16 HGNC NCBI

Linked Data

dbSNP Id: rs1908254029
gnomAD v4: 17-41612715-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612715G>A , CM000679.2:g.41612715G>A GRCh38
NC_000017.10:g.39768967G>A , CM000679.1:g.39768967G>A GRCh37
NC_000017.9:g.37022493G>A NCBI36
NG_008301.1:g.5113C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.-27C>T MANE Select ENSP00000301653.3:n.-27C>T
ENST00000301653.8:c.-27C>T ENSP00000301653.3:n.-27C>T
ENST00000588319.1:n.51C>T
ENST00000590990.1:c.-27C>T ENSP00000467105.1:n.-27C>T
ENST00000593067.1:c.-313+75C>T ENSP00000467124.1:n.-313+75C>T
NM_005557.3:c.-27C>T NP_005548.2:n.-27C>T
NM_005557.4:c.-27C>T MANE Select NP_005548.2:n.-27C>T
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