Canonical Allele Identifier: CA2260099823
Gene: KRT16 HGNC NCBI

Linked Data

dbSNP Id: rs764850876
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612538_41612541dup , CM000679.2:g.41612538_41612541dup GRCh38
NC_000017.10:g.39768790_39768793dup , CM000679.1:g.39768790_39768793dup GRCh37
NC_000017.9:g.37022316_37022319dup NCBI36
NG_008301.1:g.5293_5296dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000301653.9:c.154_157dup MANE Select ENSP00000301653.3:p.Ser53CysfsTer29
ENST00000301653.8:c.154_157dup ENSP00000301653.3:p.Ser53CysfsTer29
ENST00000588319.1:n.231_234dup
ENST00000593067.1:c.-312-249_-312-246dup ENSP00000467124.1:n.-312-249_-312-246dup
NM_005557.3:c.154_157dup NP_005548.2:p.Ser53CysfsTer29
NM_005557.4:c.154_157dup MANE Select NP_005548.2:p.Ser53CysfsTer29
Search 100 bp 5'
Search 100 bp 3'