Canonical Allele Identifier: CA500206156
Gene: KRT16 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39768671A>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612419A>C , CM000679.2:g.41612419A>C GRCh38
NC_000017.10:g.39768671A>C , CM000679.1:g.39768671A>C GRCh37
NC_000017.9:g.37022197A>C NCBI36
NG_008301.1:g.5409T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.270T>G MANE Select ENSP00000301653.3:p.Leu90=
ENST00000301653.8:c.270T>G ENSP00000301653.3:p.Leu90=
ENST00000588319.1:n.347T>G
ENST00000593067.1:c.-312-133T>G ENSP00000467124.1:n.-312-133T>G
NM_005557.3:c.270T>G NP_005548.2:p.Leu90=
NM_005557.4:c.270T>G MANE Select NP_005548.2:p.Leu90=
Search 100 bp 5'
Search 100 bp 3'