Canonical Allele Identifier: CA2260105407
Gene: KRT17 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624131_41624132delinsGC , CM000679.2:g.41624131_41624132delinsGC GRCh38
NC_000017.10:g.39780383_39780384delinsGC , CM000679.1:g.39780383_39780384delinsGC GRCh37
NC_000017.9:g.37033909_37033910delinsGC NCBI36
NG_008625.1:g.5499_5500delinsGC
NG_009090.2:g.167581_167582delinsGC , LRG_401:g.167581_167582delinsGC

Transcript Alleles

HGVS Amino-acid change
ENST00000311208.13:c.378_379delinsGC MANE Select ENSP00000308452.8:p.Gly126=
ENST00000311208.12:c.378_379delinsGC ENSP00000308452.8:p.Gly126=
ENST00000463128.5:c.-238_-237delinsGC ENSP00000468672.1:n.-238_-237delinsGC
ENST00000491673.1:n.444_445delinsGC
ENST00000493253.5:n.165_166delinsGC
ENST00000540235.5:c.129_130delinsGC ENSP00000441751.2:p.Gly43=
ENST00000577817.3:c.333_334delinsGC ENSP00000467418.1:p.Gly111=
NM_000422.2:c.378_379delinsGC NP_000413.1:p.Gly126=
NM_000422.3:c.378_379delinsGC MANE Select NP_000413.1:p.Gly126=