Canonical Allele Identifier: CA399497186
Gene: KRT16 HGNC NCBI

Linked Data

dbSNP Id: rs267607409
gnomAD v2: 17-39768898-T-C
gnomAD v4: 17-41612646-T-C
MyVariant Identifiers: chr17:g.39768898T>C (hg19) chr17:g.41612646T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612646T>C , CM000679.2:g.41612646T>C GRCh38
NC_000017.10:g.39768898T>C , CM000679.1:g.39768898T>C GRCh37
NC_000017.9:g.37022424T>C NCBI36
NG_008301.1:g.5182A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.43A>G MANE Select ENSP00000301653.3:p.Lys15Glu
ENST00000301653.8:c.43A>G ENSP00000301653.3:p.Lys15Glu
ENST00000588319.1:n.120A>G
ENST00000590990.1:c.43A>G ENSP00000467105.1:p.Lys15Glu
ENST00000593067.1:c.-313+144A>G ENSP00000467124.1:n.-313+144A>G
NM_005557.3:c.43A>G NP_005548.2:p.Lys15Glu
NM_005557.4:c.43A>G MANE Select NP_005548.2:p.Lys15Glu
Search 100 bp 5'
Search 100 bp 3'