Canonical Allele Identifier: CA2637838428
Gene: KRT16 HGNC NCBI

Linked Data

gnomAD v4: 17-41612707-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612707G>C , CM000679.2:g.41612707G>C GRCh38
NC_000017.10:g.39768959G>C , CM000679.1:g.39768959G>C GRCh37
NC_000017.9:g.37022485G>C NCBI36
NG_008301.1:g.5121C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.-19C>G MANE Select ENSP00000301653.3:n.-19C>G
ENST00000301653.8:c.-19C>G ENSP00000301653.3:n.-19C>G
ENST00000588319.1:n.59C>G
ENST00000590990.1:c.-19C>G ENSP00000467105.1:n.-19C>G
ENST00000593067.1:c.-313+83C>G ENSP00000467124.1:n.-313+83C>G
NM_005557.3:c.-19C>G NP_005548.2:n.-19C>G
NM_005557.4:c.-19C>G MANE Select NP_005548.2:n.-19C>G
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