Canonical Allele Identifier: CA2637840901

Gene: KRT17

Linked Data

• gnomAD v4: 17-41624415-G-GCCCCACCTCCTGCCCCACCTC

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624415_41624416insCCCCACCTCCTGCCCCACCTC , CM000679.2:g.41624415_41624416insCCCCACCTCCTGCCCCACCTC	GRCh38
NC_000017.10:g.39780667_39780668insCCCCACCTCCTGCCCCACCTC , CM000679.1:g.39780667_39780668insCCCCACCTCCTGCCCCACCTC	GRCh37
NC_000017.9:g.37034193_37034194insCCCCACCTCCTGCCCCACCTC	NCBI36
NG_008625.1:g.5215_5216insGAGGTGGGGCAGGAGGTGGGG
NG_009090.2:g.167297_167298insGAGGTGGGGCAGGAGGTGGGG , LRG_401:g.167297_167298insGAGGTGGGGCAGGAGGTGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.94_95insGAGGTGGGGCAGGAGGTGGGG MANE Select	ENSP00000308452.8:p.Ser32Ter
ENST00000311208.12:c.94_95insGAGGTGGGGCAGGAGGTGGGG	ENSP00000308452.8:p.Ser32Ter
ENST00000463128.5:c.-312-210_-312-209insGAGGTGGGGCAGGAGGTGGGG	ENSP00000468672.1:n.-312-210_-312-209insGAGGTGGGGCAGGAGGTGGGG...
ENST00000491673.1:n.160_161insGAGGTGGGGCAGGAGGTGGGG
ENST00000540235.5:c.-112_-111insGAGGTGGGGCAGGAGGTGGGG	ENSP00000441751.2:n.-112_-111insGAGGTGGGGCAGGAGGTGGGG
ENST00000577817.3:c.49_50insGAGGTGGGGCAGGAGGTGGGG	ENSP00000467418.1:p.Ser17Ter
NM_000422.2:c.94_95insGAGGTGGGGCAGGAGGTGGGG	NP_000413.1:p.Ser32Ter
NM_000422.3:c.94_95insGAGGTGGGGCAGGAGGTGGGG MANE Select	NP_000413.1:p.Ser32Ter