Canonical Allele Identifier: CA399496158
Gene: KRT16 HGNC NCBI

Linked Data

dbSNP Id: rs1445424962

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612525C>G , CM000679.2:g.41612525C>G GRCh38
NC_000017.10:g.39768777C>G , CM000679.1:g.39768777C>G GRCh37
NC_000017.9:g.37022303C>G NCBI36
NG_008301.1:g.5303G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.164G>C MANE Select ENSP00000301653.3:p.Arg55Pro
ENST00000301653.8:c.164G>C ENSP00000301653.3:p.Arg55Pro
ENST00000588319.1:n.241G>C
ENST00000593067.1:c.-312-239G>C ENSP00000467124.1:n.-312-239G>C
NM_005557.3:c.164G>C NP_005548.2:p.Arg55Pro
NM_005557.4:c.164G>C MANE Select NP_005548.2:p.Arg55Pro