Canonical Allele Identifier: CA500205518
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs1907425482
MyVariant Identifiers: chr17:g.39740072G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583820G>A , CM000679.2:g.41583820G>A GRCh38
NC_000017.10:g.39740072G>A , CM000679.1:g.39740072G>A GRCh37
NC_000017.9:g.36993598G>A NCBI36
NG_008624.1:g.8076C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.867C>T MANE Select ENSP00000167586.6:p.Asp289=
ENST00000167586.6:c.867C>T ENSP00000167586.6:p.Asp289=
ENST00000476662.1:n.317C>T
NM_000526.4:c.867C>T NP_000517.2:p.Asp289=
NM_000526.5:c.867C>T MANE Select NP_000517.3:p.Asp289=