Canonical Allele Identifier: CA399511542

Gene: KRT17

Linked Data

• MyVariant Identifiers: chr17:g.39780347C>A (hg19) ; chr17:g.41624095C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624095C>A , CM000679.2:g.41624095C>A	GRCh38
NC_000017.10:g.39780347C>A , CM000679.1:g.39780347C>A	GRCh37
NC_000017.9:g.37033873C>A	NCBI36
NG_008625.1:g.5536G>T
NG_009090.2:g.167618G>T , LRG_401:g.167618G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.415G>T MANE Select	ENSP00000308452.8:p.Glu139Ter
ENST00000311208.12:c.415G>T	ENSP00000308452.8:p.Glu139Ter
ENST00000463128.5:c.-201G>T	ENSP00000468672.1:n.-201G>T
ENST00000491673.1:n.481G>T
ENST00000493253.5:n.202G>T
ENST00000540235.5:c.166G>T	ENSP00000441751.2:p.Glu56Ter
ENST00000577817.3:c.370G>T	ENSP00000467418.1:p.Glu124Ter
NM_000422.2:c.415G>T	NP_000413.1:p.Glu139Ter
NM_000422.3:c.415G>T MANE Select	NP_000413.1:p.Glu139Ter