Canonical Allele Identifier: CA500012336

Gene: KRT17

Linked Data

• MyVariant Identifiers: chr17:g.39780723G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624471G>T , CM000679.2:g.41624471G>T	GRCh38
NC_000017.10:g.39780723G>T , CM000679.1:g.39780723G>T	GRCh37
NC_000017.9:g.37034249G>T	NCBI36
NG_008625.1:g.5160C>A
NG_009090.2:g.167242C>A , LRG_401:g.167242C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.39C>A MANE Select	ENSP00000308452.8:p.Ser13=
ENST00000311208.12:c.39C>A	ENSP00000308452.8:p.Ser13=
ENST00000463128.5:c.-312-265C>A	ENSP00000468672.1:n.-312-265C>A
ENST00000491673.1:n.105C>A
ENST00000540235.5:c.-167C>A	ENSP00000441751.2:n.-167C>A
NM_000422.2:c.39C>A	NP_000413.1:p.Ser13=
NM_000422.3:c.39C>A MANE Select	NP_000413.1:p.Ser13=