Canonical Allele Identifier: CA500206201

Gene: KRT17

Linked Data

• MyVariant Identifiers: chr17:g.39780392_39780393insG (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624140_41624141insG , CM000679.2:g.41624140_41624141insG	GRCh38
NC_000017.10:g.39780392_39780393insG , CM000679.1:g.39780392_39780393insG	GRCh37
NC_000017.9:g.37033918_37033919insG	NCBI36
NG_008625.1:g.5490_5491insC
NG_009090.2:g.167572_167573insC , LRG_401:g.167572_167573insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.369_370insC MANE Select	ENSP00000308452.8:p.Ala124ArgfsTer7
ENST00000311208.12:c.369_370insC	ENSP00000308452.8:p.Ala124ArgfsTer7
ENST00000463128.5:c.-247_-246insC	ENSP00000468672.1:n.-247_-246insC
ENST00000491673.1:n.435_436insC
ENST00000493253.5:n.156_157insC
ENST00000540235.5:c.120_121insC	ENSP00000441751.2:p.Ala41ArgfsTer7
ENST00000577817.3:c.324_325insC	ENSP00000467418.1:p.Ala109ArgfsTer7
NM_000422.2:c.369_370insC	NP_000413.1:p.Ala124ArgfsTer7
NM_000422.3:c.369_370insC MANE Select	NP_000413.1:p.Ala124ArgfsTer7