Canonical Allele Identifier: CA2809496903

Gene: KRT17

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624291_41624292insCCCAAACACACCCAACAC , CM000679.2:g.41624291_41624292insCCCAAACACACCCAACAC	GRCh38
NC_000017.10:g.39780543_39780544insCCCAAACACACCCAACAC , CM000679.1:g.39780543_39780544insCCCAAACACACCCAACAC	GRCh37
NC_000017.9:g.37034069_37034070insCCCAAACACACCCAACAC	NCBI36
NG_008625.1:g.5339_5340insGTGTTGGGTGTGTTTGGG
NG_009090.2:g.167421_167422insGTGTTGGGTGTGTTTGGG , LRG_401:g.167421_167422insGTGTTGGGTGTGTTTGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.218_219insGTGTTGGGTGTGTTTGGG MANE Select	ENSP00000308452.8:p.Phe73delinsLeuCysTrpValCysLeuGly
ENST00000311208.12:c.218_219insGTGTTGGGTGTGTTTGGG	ENSP00000308452.8:p.Phe73delinsLeuCysTrpValCysLeuGly
ENST00000463128.5:c.-312-86_-312-85insGTGTTGGGTGTGTTTGGG	ENSP00000468672.1:n.-312-86_-312-85insGTGTTGGGTGTGTTTGGG
ENST00000491673.1:n.284_285insGTGTTGGGTGTGTTTGGG
ENST00000493253.5:n.5_6insGTGTTGGGTGTGTTTGGG
ENST00000540235.5:c.13_14insGTGTTGGGTGTGTTTGGG	ENSP00000441751.2:p.Leu5delinsCysValGlyCysValTrpVal
ENST00000577817.3:c.173_174insGTGTTGGGTGTGTTTGGG	ENSP00000467418.1:p.Phe58delinsLeuCysTrpValCysLeuGly
NM_000422.2:c.218_219insGTGTTGGGTGTGTTTGGG	NP_000413.1:p.Phe73delinsLeuCysTrpValCysLeuGly
NM_000422.3:c.218_219insGTGTTGGGTGTGTTTGGG MANE Select	NP_000413.1:p.Phe73delinsLeuCysTrpValCysLeuGly