Canonical Allele Identifier: CA500206280

Gene: KRT17

Linked Data

• MyVariant Identifiers: chr17:g.39780449G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624197G>A , CM000679.2:g.41624197G>A	GRCh38
NC_000017.10:g.39780449G>A , CM000679.1:g.39780449G>A	GRCh37
NC_000017.9:g.37033975G>A	NCBI36
NG_008625.1:g.5434C>T
NG_009090.2:g.167516C>T , LRG_401:g.167516C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.313C>T MANE Select	ENSP00000308452.8:p.Leu105=
ENST00000311208.12:c.313C>T	ENSP00000308452.8:p.Leu105=
ENST00000463128.5:c.-303C>T	ENSP00000468672.1:n.-303C>T
ENST00000491673.1:n.379C>T
ENST00000493253.5:n.100C>T
ENST00000540235.5:c.72-6C>T	ENSP00000441751.2:n.72-6C>T
ENST00000577817.3:c.268C>T	ENSP00000467418.1:p.Leu90=
NM_000422.2:c.313C>T	NP_000413.1:p.Leu105=
NM_000422.3:c.313C>T MANE Select	NP_000413.1:p.Leu105=