Canonical Allele Identifier: CA500206558
Gene: KRT16 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39768551G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612299G>T , CM000679.2:g.41612299G>T GRCh38
NC_000017.10:g.39768551G>T , CM000679.1:g.39768551G>T GRCh37
NC_000017.9:g.37022077G>T NCBI36
NG_008301.1:g.5529C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.390C>A MANE Select ENSP00000301653.3:p.Ser130=
ENST00000301653.8:c.390C>A ENSP00000301653.3:p.Ser130=
ENST00000588319.1:n.467C>A
ENST00000593067.1:c.-312-13C>A ENSP00000467124.1:n.-312-13C>A
NM_005557.3:c.390C>A NP_005548.2:p.Ser130=
NM_005557.4:c.390C>A MANE Select NP_005548.2:p.Ser130=