Canonical Allele Identifier: CA2637838448
Gene: KRT16 HGNC NCBI

Linked Data

gnomAD v4: 17-41612721-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612721T>C , CM000679.2:g.41612721T>C GRCh38
NC_000017.10:g.39768973T>C , CM000679.1:g.39768973T>C GRCh37
NC_000017.9:g.37022499T>C NCBI36
NG_008301.1:g.5107A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.-33A>G MANE Select ENSP00000301653.3:n.-33A>G
ENST00000301653.8:c.-33A>G ENSP00000301653.3:n.-33A>G
ENST00000588319.1:n.45A>G
ENST00000590990.1:c.-33A>G ENSP00000467105.1:n.-33A>G
ENST00000593067.1:c.-313+69A>G ENSP00000467124.1:n.-313+69A>G
NM_005557.3:c.-33A>G NP_005548.2:n.-33A>G
NM_005557.4:c.-33A>G MANE Select NP_005548.2:n.-33A>G
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