Canonical Allele Identifier: CA290677579
Gene: KRT16 HGNC NCBI

Linked Data

dbSNP Id: rs142288943
COSMIC: COSM110545
MyVariant Identifiers: chr17:g.39768494G>A (hg19) chr17:g.41612242G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612242G>A , CM000679.2:g.41612242G>A GRCh38
NC_000017.10:g.39768494G>A , CM000679.1:g.39768494G>A GRCh37
NC_000017.9:g.37022020G>A NCBI36
NG_008301.1:g.5586C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.447C>T MANE Select ENSP00000301653.3:p.Ile149=
ENST00000301653.8:c.447C>T ENSP00000301653.3:p.Ile149=
ENST00000588319.1:n.524C>T
ENST00000593067.1:c.-268C>T ENSP00000467124.1:n.-268C>T
NM_005557.3:c.447C>T NP_005548.2:p.Ile149=
NM_005557.4:c.447C>T MANE Select NP_005548.2:p.Ile149=
Search 100 bp 5'
Search 100 bp 3'