Canonical Allele Identifier: CA399511589

Gene: KRT17

Linked Data

• MyVariant Identifiers: chr17:g.39780352G>T (hg19) ; chr17:g.41624100G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624100G>T , CM000679.2:g.41624100G>T	GRCh38
NC_000017.10:g.39780352G>T , CM000679.1:g.39780352G>T	GRCh37
NC_000017.9:g.37033878G>T	NCBI36
NG_008625.1:g.5531C>A
NG_009090.2:g.167613C>A , LRG_401:g.167613C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.410C>A MANE Select	ENSP00000308452.8:p.Thr137Lys
ENST00000311208.12:c.410C>A	ENSP00000308452.8:p.Thr137Lys
ENST00000463128.5:c.-206C>A	ENSP00000468672.1:n.-206C>A
ENST00000491673.1:n.476C>A
ENST00000493253.5:n.197C>A
ENST00000540235.5:c.161C>A	ENSP00000441751.2:p.Thr54Lys
ENST00000577817.3:c.365C>A	ENSP00000467418.1:p.Thr122Lys
NM_000422.2:c.410C>A	NP_000413.1:p.Thr137Lys
NM_000422.3:c.410C>A MANE Select	NP_000413.1:p.Thr137Lys