Canonical Allele Identifier: CA2637838455
Gene: KRT16 HGNC NCBI

Linked Data

gnomAD v4: 17-41612729-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612729A>G , CM000679.2:g.41612729A>G GRCh38
NC_000017.10:g.39768981A>G , CM000679.1:g.39768981A>G GRCh37
NC_000017.9:g.37022507A>G NCBI36
NG_008301.1:g.5099T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.-41T>C MANE Select ENSP00000301653.3:n.-41T>C
ENST00000301653.8:c.-41T>C ENSP00000301653.3:n.-41T>C
ENST00000588319.1:n.37T>C
ENST00000590990.1:c.-36-5T>C ENSP00000467105.1:n.-36-5T>C
ENST00000593067.1:c.-313+61T>C ENSP00000467124.1:n.-313+61T>C
NM_005557.3:c.-41T>C NP_005548.2:n.-41T>C
NM_005557.4:c.-41T>C MANE Select NP_005548.2:n.-41T>C
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