Canonical Allele Identifier: CA399495859
Gene: KRT16 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39768730C>A (hg19) chr17:g.41612478C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612478C>A , CM000679.2:g.41612478C>A GRCh38
NC_000017.10:g.39768730C>A , CM000679.1:g.39768730C>A GRCh37
NC_000017.9:g.37022256C>A NCBI36
NG_008301.1:g.5350G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.211G>T MANE Select ENSP00000301653.3:p.Gly71Cys
ENST00000301653.8:c.211G>T ENSP00000301653.3:p.Gly71Cys
ENST00000588319.1:n.288G>T
ENST00000593067.1:c.-312-192G>T ENSP00000467124.1:n.-312-192G>T
NM_005557.3:c.211G>T NP_005548.2:p.Gly71Cys
NM_005557.4:c.211G>T MANE Select NP_005548.2:p.Gly71Cys
Search 100 bp 5'
Search 100 bp 3'