Canonical Allele Identifier: CA2260099704
Gene: KRT16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612327A= , CM000679.2:g.41612327A= GRCh38
NC_000017.10:g.39768579A= , CM000679.1:g.39768579A= GRCh37
NC_000017.9:g.37022105A= NCBI36
NG_008301.1:g.5501T=

Transcript Alleles

HGVS Amino-acid change
ENST00000301653.9:c.362T= MANE Select ENSP00000301653.3:p.Met121=
ENST00000301653.8:c.362T= ENSP00000301653.3:p.Met121=
ENST00000588319.1:n.439T=
ENST00000593067.1:c.-312-41T= ENSP00000467124.1:n.-312-41T=
NM_005557.3:c.362T= NP_005548.2:p.Met121=
NM_005557.4:c.362T= MANE Select NP_005548.2:p.Met121=