Canonical Allele Identifier: CA2637838476
Gene: KRT16 HGNC NCBI

Linked Data

gnomAD v4: 17-41612761-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612761G>C , CM000679.2:g.41612761G>C GRCh38
NC_000017.10:g.39769013G>C , CM000679.1:g.39769013G>C GRCh37
NC_000017.9:g.37022539G>C NCBI36
NG_008301.1:g.5067C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.-73C>G MANE Select ENSP00000301653.3:n.-73C>G
ENST00000588319.1:n.5C>G
ENST00000590990.1:c.-36-37C>G ENSP00000467105.1:n.-36-37C>G
ENST00000593067.1:c.-313+29C>G ENSP00000467124.1:n.-313+29C>G
NM_005557.3:c.-73C>G NP_005548.2:n.-73C>G
NM_005557.4:c.-73C>G MANE Select NP_005548.2:n.-73C>G
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