Canonical Allele Identifier: CA2576267853
Gene: KRT16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612707G>A , CM000679.2:g.41612707G>A GRCh38
NC_000017.10:g.39768959G>A , CM000679.1:g.39768959G>A GRCh37
NC_000017.9:g.37022485G>A NCBI36
NG_008301.1:g.5121C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.-19C>T MANE Select ENSP00000301653.3:n.-19C>T
ENST00000301653.8:c.-19C>T ENSP00000301653.3:n.-19C>T
ENST00000588319.1:n.59C>T
ENST00000590990.1:c.-19C>T ENSP00000467105.1:n.-19C>T
ENST00000593067.1:c.-313+83C>T ENSP00000467124.1:n.-313+83C>T
NM_005557.3:c.-19C>T NP_005548.2:n.-19C>T
NM_005557.4:c.-19C>T MANE Select NP_005548.2:n.-19C>T