Canonical Allele Identifier: CA500206471
Gene: KRT16 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39768488G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612236G>A , CM000679.2:g.41612236G>A GRCh38
NC_000017.10:g.39768488G>A , CM000679.1:g.39768488G>A GRCh37
NC_000017.9:g.37022014G>A NCBI36
NG_008301.1:g.5592C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.453C>T MANE Select ENSP00000301653.3:p.Asp151=
ENST00000301653.8:c.453C>T ENSP00000301653.3:p.Asp151=
ENST00000588319.1:n.530C>T
ENST00000593067.1:c.-262C>T ENSP00000467124.1:n.-262C>T
NM_005557.3:c.453C>T NP_005548.2:p.Asp151=
NM_005557.4:c.453C>T MANE Select NP_005548.2:p.Asp151=