Canonical Allele Identifier: CA2036598497
Gene: KRT2 HGNC NCBI

Linked Data

dbSNP Id: rs749353054
gnomAD v4: 12-52651990-C-CCCG
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52651993_52651995dup , CM000674.2:g.52651993_52651995dup GRCh38
NC_000012.11:g.53045777_53045779dup , CM000674.1:g.53045777_53045779dup GRCh37
NC_000012.10:g.51332044_51332046dup NCBI36
NG_008296.1:g.5183_5185dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000309680.4:c.150_152dup MANE Select ENSP00000310861.3:p.Gly51_Gly52insGly
ENST00000309680.3:c.150_152dup ENSP00000310861.3:p.Gly51_Gly52insGly
NM_000423.2:c.150_152dup NP_000414.2:p.Gly51_Gly52insGly
NM_000423.3:c.150_152dup MANE Select NP_000414.2:p.Gly51_Gly52insGly
Search 100 bp 5'
Search 100 bp 3'