Canonical Allele Identifier: CA2576267857
Gene: KRT16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612723G>A , CM000679.2:g.41612723G>A GRCh38
NC_000017.10:g.39768975G>A , CM000679.1:g.39768975G>A GRCh37
NC_000017.9:g.37022501G>A NCBI36
NG_008301.1:g.5105C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.-35C>T MANE Select ENSP00000301653.3:n.-35C>T
ENST00000301653.8:c.-35C>T ENSP00000301653.3:n.-35C>T
ENST00000588319.1:n.43C>T
ENST00000590990.1:c.-35C>T ENSP00000467105.1:n.-35C>T
ENST00000593067.1:c.-313+67C>T ENSP00000467124.1:n.-313+67C>T
NM_005557.3:c.-35C>T NP_005548.2:n.-35C>T
NM_005557.4:c.-35C>T MANE Select NP_005548.2:n.-35C>T