Canonical Allele Identifier: CA217377
Gene: KRT16 HGNC NCBI

Linked Data

ClinVar Variation Id: 14608
ClinVar RCV Id: RCV000015712 RCV000057030 RCV002496376
dbSNP Id: rs28928894
MyVariant Identifiers: chr17:g.39768579A>G (hg19) chr17:g.41612327A>G (hg38)
PubMed: PMID:11886499
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612327A>G , CM000679.2:g.41612327A>G GRCh38
NC_000017.10:g.39768579A>G , CM000679.1:g.39768579A>G GRCh37
NC_000017.9:g.37022105A>G NCBI36
NG_008301.1:g.5501T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000301653.9:c.362T>C MANE Select ENSP00000301653.3:p.Met121Thr
ENST00000301653.8:c.362T>C ENSP00000301653.3:p.Met121Thr
ENST00000588319.1:n.439T>C
ENST00000593067.1:c.-312-41T>C ENSP00000467124.1:n.-312-41T>C
NM_005557.3:c.362T>C NP_005548.2:p.Met121Thr
NM_005557.4:c.362T>C MANE Select NP_005548.2:p.Met121Thr
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Search 100 bp 3'