Canonical Allele Identifier: CA290677767
Gene: KRT16 HGNC NCBI

Linked Data

dbSNP Id: rs121912477

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000301653.9:c.368A>G MANE Select ENSP00000301653.3:p.Asn123Ser
ENST00000301653.8:c.368A>G ENSP00000301653.3:p.Asn123Ser
ENST00000588319.1:n.445A>G
ENST00000593067.1:c.-312-35A>G ENSP00000467124.1:n.-312-35A>G
NM_005557.3:c.368A>G NP_005548.2:p.Asn123Ser
NM_005557.4:c.368A>G MANE Select NP_005548.2:p.Asn123Ser