Canonical Allele Identifier: CA2260105508

Gene: KRT17

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624295_41624296delinsCT , CM000679.2:g.41624295_41624296delinsCT	GRCh38
NC_000017.10:g.39780547_39780548delinsCT , CM000679.1:g.39780547_39780548delinsCT	GRCh37
NC_000017.9:g.37034073_37034074delinsCT	NCBI36
NG_008625.1:g.5335_5336delinsAG
NG_009090.2:g.167417_167418delinsAG , LRG_401:g.167417_167418delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.214_215delinsAG MANE Select	ENSP00000308452.8:p.Ser72=
ENST00000311208.12:c.214_215delinsAG	ENSP00000308452.8:p.Ser72=
ENST00000463128.5:c.-312-90_-312-89delinsAG	ENSP00000468672.1:n.-312-90_-312-89delinsAG
ENST00000491673.1:n.280_281delinsAG
ENST00000493253.5:n.1_2delinsAG
ENST00000540235.5:c.9_10delinsAG	ENSP00000441751.2:p.Ala3=
ENST00000577817.3:c.169_170delinsAG	ENSP00000467418.1:p.Ser57=
NM_000422.2:c.214_215delinsAG	NP_000413.1:p.Ser72=
NM_000422.3:c.214_215delinsAG MANE Select	NP_000413.1:p.Ser72=