Canonical Allele Identifier: CA399497551
Gene: KRT16 HGNC NCBI

Linked Data

ClinVar Variation Id: 2614868
ClinVar RCV Id: RCV003365014
MyVariant Identifiers: chr17:g.39768931A>C (hg19) chr17:g.41612679A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612679A>C , CM000679.2:g.41612679A>C GRCh38
NC_000017.10:g.39768931A>C , CM000679.1:g.39768931A>C GRCh37
NC_000017.9:g.37022457A>C NCBI36
NG_008301.1:g.5149T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.10T>G MANE Select ENSP00000301653.3:p.Cys4Gly
ENST00000301653.8:c.10T>G ENSP00000301653.3:p.Cys4Gly
ENST00000588319.1:n.87T>G
ENST00000590990.1:c.10T>G ENSP00000467105.1:p.Cys4Gly
ENST00000593067.1:c.-313+111T>G ENSP00000467124.1:n.-313+111T>G
NM_005557.3:c.10T>G NP_005548.2:p.Cys4Gly
NM_005557.4:c.10T>G MANE Select NP_005548.2:p.Cys4Gly
Search 100 bp 5'
Search 100 bp 3'