Canonical Allele Identifier: CA500206072

Gene: KRT17

Linked Data

• MyVariant Identifiers: chr17:g.39780351T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624099T>A , CM000679.2:g.41624099T>A	GRCh38
NC_000017.10:g.39780351T>A , CM000679.1:g.39780351T>A	GRCh37
NC_000017.9:g.37033877T>A	NCBI36
NG_008625.1:g.5532A>T
NG_009090.2:g.167614A>T , LRG_401:g.167614A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.411A>T MANE Select	ENSP00000308452.8:p.Thr137=
ENST00000311208.12:c.411A>T	ENSP00000308452.8:p.Thr137=
ENST00000463128.5:c.-205A>T	ENSP00000468672.1:n.-205A>T
ENST00000491673.1:n.477A>T
ENST00000493253.5:n.198A>T
ENST00000540235.5:c.162A>T	ENSP00000441751.2:p.Thr54=
ENST00000577817.3:c.366A>T	ENSP00000467418.1:p.Thr122=
NM_000422.2:c.411A>T	NP_000413.1:p.Thr137=
NM_000422.3:c.411A>T MANE Select	NP_000413.1:p.Thr137=