Canonical Allele Identifier: CA399512042

Gene: KRT17

Linked Data

• dbSNP Id: rs1908643107
• MyVariant Identifiers: chr17:g.39780405C>A (hg19) ; chr17:g.41624153C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624153C>A , CM000679.2:g.41624153C>A	GRCh38
NC_000017.10:g.39780405C>A , CM000679.1:g.39780405C>A	GRCh37
NC_000017.9:g.37033931C>A	NCBI36
NG_008625.1:g.5478G>T
NG_009090.2:g.167560G>T , LRG_401:g.167560G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.357G>T MANE Select	ENSP00000308452.8:p.Trp119Cys
ENST00000311208.12:c.357G>T	ENSP00000308452.8:p.Trp119Cys
ENST00000463128.5:c.-259G>T	ENSP00000468672.1:n.-259G>T
ENST00000491673.1:n.423G>T
ENST00000493253.5:n.144G>T
ENST00000540235.5:c.108G>T	ENSP00000441751.2:p.Trp36Cys
ENST00000577817.3:c.312G>T	ENSP00000467418.1:p.Trp104Cys
NM_000422.2:c.357G>T	NP_000413.1:p.Trp119Cys
NM_000422.3:c.357G>T MANE Select	NP_000413.1:p.Trp119Cys