Canonical Allele Identifier: CA2036663532
Gene: KRT4 HGNC NCBI

Linked Data

dbSNP Id: rs1939962442
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52813976_52813977insTGGTGG , CM000674.2:g.52813976_52813977insTGGTGG GRCh38
NC_000012.11:g.53207760_53207761insTGGTGG , CM000674.1:g.53207760_53207761insTGGTGG GRCh37
NC_000012.10:g.51494027_51494028insTGGTGG NCBI36
NG_007380.1:g.5575_5576insCCACCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.2:c.82_83insCCACCA MANE Select ENSP00000448220.1:p.Gly28delinsAlaThrSer
ENST00000548097.5:c.82_83insCCACCA ENSP00000449755.1:p.Gly28delinsAlaThrSer
ENST00000551956.1:c.82_83insCCACCA ENSP00000448220.1:p.Gly28delinsAlaThrSer
ENST00000552668.1:c.82_83insCCACCA ENSP00000447320.1:p.Gly28delinsAlaThrSer
NM_002272.3:c.82_83insCCACCA NP_002263.3:p.Gly28delinsAlaThrSer
NM_002272.4:c.82_83insCCACCA MANE Select NP_002263.3:p.Gly28delinsAlaThrSer
Search 100 bp 5'
Search 100 bp 3'