Canonical Allele Identifier: CA399511879

Gene: KRT17

Linked Data

• dbSNP Id: rs1555575055
• MyVariant Identifiers: chr17:g.39780385_39780391del (hg19) ; chr17:g.41624134_41624140del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624135_41624141del , CM000679.2:g.41624135_41624141del	GRCh38
NC_000017.10:g.39780387_39780393del , CM000679.1:g.39780387_39780393del	GRCh37
NC_000017.9:g.37033913_37033919del	NCBI36
NG_008625.1:g.5492_5498del
NG_009090.2:g.167574_167580del , LRG_401:g.167574_167580del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.371_377del MANE Select	ENSP00000308452.8:p.Ala124GlyfsTer?
ENST00000311208.12:c.371_377del	ENSP00000308452.8:p.Ala124GlyfsTer?
ENST00000463128.5:c.-245_-239del	ENSP00000468672.1:n.-245_-239del
ENST00000491673.1:n.437_443del
ENST00000493253.5:n.158_164del
ENST00000540235.5:c.122_128del	ENSP00000441751.2:p.Ala41GlyfsTer?
ENST00000577817.3:c.326_332del	ENSP00000467418.1:p.Ala109GlyfsTer?
NM_000422.2:c.371_377del	NP_000413.1:p.Ala124GlyfsTer?
NM_000422.3:c.371_377del MANE Select	NP_000413.1:p.Ala124GlyfsTer?