Canonical Allele Identifier: CA2260105655
Gene: KRT17 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624532C= , CM000679.2:g.41624532C= GRCh38
NC_000017.10:g.39780784C= , CM000679.1:g.39780784C= GRCh37
NC_000017.9:g.37034310C= NCBI36
NG_008625.1:g.5099G=
NG_009090.2:g.167181G= , LRG_401:g.167181G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000311208.13:c.-23G= MANE Select ENSP00000308452.8:n.-23G=
ENST00000311208.12:c.-23G= ENSP00000308452.8:n.-23G=
ENST00000463128.5:c.-313+211G= ENSP00000468672.1:n.-313+211G=
ENST00000491673.1:n.44G=
ENST00000540235.5:c.-228G= ENSP00000441751.2:n.-228G=
NM_000422.2:c.-23G= NP_000413.1:n.-23G=
NM_000422.3:c.-23G= MANE Select NP_000413.1:n.-23G=
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