Canonical Allele Identifier: CA2637838417
Gene: KRT16 HGNC NCBI

Linked Data

gnomAD v4: 17-41612699-A-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612699A>G , CM000679.2:g.41612699A>G GRCh38
NC_000017.10:g.39768951A>G , CM000679.1:g.39768951A>G GRCh37
NC_000017.9:g.37022477A>G NCBI36
NG_008301.1:g.5129T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.-11T>C MANE Select ENSP00000301653.3:n.-11T>C
ENST00000301653.8:c.-11T>C ENSP00000301653.3:n.-11T>C
ENST00000588319.1:n.67T>C
ENST00000590990.1:c.-11T>C ENSP00000467105.1:n.-11T>C
ENST00000593067.1:c.-313+91T>C ENSP00000467124.1:n.-313+91T>C
NM_005557.3:c.-11T>C NP_005548.2:n.-11T>C
NM_005557.4:c.-11T>C MANE Select NP_005548.2:n.-11T>C
Search 100 bp 5'
Search 100 bp 3'