Canonical Allele Identifier: CA8562759

Gene: KRT14

Linked Data

• dbSNP Id: rs746954535
• ExAC: 17:39742799 C / CAAGCCACCACCG
• gnomAD v2: 17-39742799-C-CAAGCCACCACCG
• gnomAD v3: 17-41586547-C-CAAGCCACCACCG
• gnomAD v4: 17-41586547-C-CAAGCCACCACCG
• MyVariant Identifiers: chr17:g.39742799_39742800insAAGCCACCACCG (hg19) ; chr17:g.41586547_41586548insAAGCCACCACCG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41586553_41586554insCCACCGAAGCCA , CM000679.2:g.41586553_41586554insCCACCGAAGCCA	GRCh38
NC_000017.10:g.39742805_39742806insCCACCGAAGCCA , CM000679.1:g.39742805_39742806insCCACCGAAGCCA	GRCh37
NC_000017.9:g.36996331_36996332insCCACCGAAGCCA	NCBI36
NG_008624.1:g.5348_5349insCGGTGGTGGCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000167586.7:c.287_288insCGGTGGTGGCTT MANE Select	ENSP00000167586.6:p.Gly95_Leu96insPheGlyGlyGly
ENST00000167586.6:c.287_288insCGGTGGTGGCTT	ENSP00000167586.6:p.Gly95_Leu96insPheGlyGlyGly
NM_000526.4:c.287_288insCGGTGGTGGCTT	NP_000517.2:p.Gly95_Leu96insPheGlyGlyGly
NM_000526.5:c.287_288insCGGTGGTGGCTT MANE Select	NP_000517.3:p.Gly95_Leu96insPheGlyGlyGly