Canonical Allele Identifier: CA2260099701
Gene: KRT16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612321T= , CM000679.2:g.41612321T= GRCh38
NC_000017.10:g.39768573T= , CM000679.1:g.39768573T= GRCh37
NC_000017.9:g.37022099T= NCBI36
NG_008301.1:g.5507A=

Transcript Alleles

HGVS Amino-acid change
ENST00000301653.9:c.368A= MANE Select ENSP00000301653.3:p.Asn123=
ENST00000301653.8:c.368A= ENSP00000301653.3:p.Asn123=
ENST00000588319.1:n.445A=
ENST00000593067.1:c.-312-35A= ENSP00000467124.1:n.-312-35A=
NM_005557.3:c.368A= NP_005548.2:p.Asn123=
NM_005557.4:c.368A= MANE Select NP_005548.2:p.Asn123=