Canonical Allele Identifier: CA399497569
Gene: KRT16 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612679A>G , CM000679.2:g.41612679A>G GRCh38
NC_000017.10:g.39768931A>G , CM000679.1:g.39768931A>G GRCh37
NC_000017.9:g.37022457A>G NCBI36
NG_008301.1:g.5149T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.10T>C MANE Select ENSP00000301653.3:p.Cys4Arg
ENST00000301653.8:c.10T>C ENSP00000301653.3:p.Cys4Arg
ENST00000588319.1:n.87T>C
ENST00000590990.1:c.10T>C ENSP00000467105.1:p.Cys4Arg
ENST00000593067.1:c.-313+111T>C ENSP00000467124.1:n.-313+111T>C
NM_005557.3:c.10T>C NP_005548.2:p.Cys4Arg
NM_005557.4:c.10T>C MANE Select NP_005548.2:p.Cys4Arg