Canonical Allele Identifier: CA645571515
Gene: KRT2 HGNC NCBI

Linked Data

COSMIC: COSM4589614
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52651851_52651852insCCAAAGCCGCTGCCGCCT , CM000674.2:g.52651851_52651852insCCAAAGCCGCTGCCGCCT GRCh38
NC_000012.11:g.53045635_53045636insCCAAAGCCGCTGCCGCCT , CM000674.1:g.53045635_53045636insCCAAAGCCGCTGCCGCCT GRCh37
NC_000012.10:g.51331902_51331903insCCAAAGCCGCTGCCGCCT NCBI36
NG_008296.1:g.5324_5325insAGGCGGCAGCGGCTTTGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000309680.4:c.291_292insAGGCGGCAGCGGCTTTGG MANE Select ENSP00000310861.3:p.Gly97_Gly98insArgArgGlnArgLeuTrp
ENST00000309680.3:c.291_292insAGGCGGCAGCGGCTTTGG ENSP00000310861.3:p.Gly97_Gly98insArgArgGlnArgLeuTrp
NM_000423.2:c.291_292insAGGCGGCAGCGGCTTTGG NP_000414.2:p.Gly97_Gly98insArgArgGlnArgLeuTrp
NM_000423.3:c.291_292insAGGCGGCAGCGGCTTTGG MANE Select NP_000414.2:p.Gly97_Gly98insArgArgGlnArgLeuTrp
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