Canonical Allele Identifier: CA290685799

Gene: KRT17

Linked Data

• dbSNP Id: rs1013390637
• gnomAD v3: 17-41623889-T-TGCTGTCCCCAGAAAAGGG
• gnomAD v4: 17-41623889-T-TGCTGTCCCCAGAAAAGGG
• MyVariant Identifiers: chr17:g.39780141_39780142insGCTGTCCCCAGAAAAGGG (hg19) ; chr17:g.41623889_41623890insGCTGTCCCCAGAAAAGGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41623891_41623908dup , CM000679.2:g.41623891_41623908dup	GRCh38
NC_000017.10:g.39780143_39780160dup , CM000679.1:g.39780143_39780160dup	GRCh37
NC_000017.9:g.37033669_37033686dup	NCBI36
NG_008625.1:g.5724_5741dup
NG_009090.2:g.167806_167823dup , LRG_401:g.167806_167823dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.432+171_432+188dup MANE Select	ENSP00000308452.8:n.432+171_432+188dup
ENST00000311208.12:c.432+171_432+188dup	ENSP00000308452.8:n.432+171_432+188dup
ENST00000463128.5:c.-184+171_-184+188dup	ENSP00000468672.1:n.-184+171_-184+188dup
ENST00000491673.1:n.498+171_498+188dup
ENST00000493253.5:n.219+171_219+188dup
ENST00000540235.5:c.183+171_183+188dup	ENSP00000441751.2:n.183+171_183+188dup
ENST00000577817.3:c.387+171_387+188dup	ENSP00000467418.1:n.387+171_387+188dup
NM_000422.2:c.432+171_432+188dup	NP_000413.1:n.432+171_432+188dup
NM_000422.3:c.432+171_432+188dup MANE Select	NP_000413.1:n.432+171_432+188dup