Canonical Allele Identifier: CA2260105450

Gene: KRT17

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624206_41624215delinsCCTTGTCCAG , CM000679.2:g.41624206_41624215delinsCCTTGTCCAG	GRCh38
NC_000017.10:g.39780458_39780467delinsCCTTGTCCAG , CM000679.1:g.39780458_39780467delinsCCTTGTCCAG	GRCh37
NC_000017.9:g.37033984_37033993delinsCCTTGTCCAG	NCBI36
NG_008625.1:g.5416_5425delinsCTGGACAAGG
NG_009090.2:g.167498_167507delinsCTGGACAAGG , LRG_401:g.167498_167507delinsCTGGACAAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.295_304delinsCTGGACAAGG MANE Select	ENSP00000308452.8:p.Leu99=
ENST00000311208.12:c.295_304delinsCTGGACAAGG	ENSP00000308452.8:p.Leu99=
ENST00000463128.5:c.-312-9_-312delinsCTGGACAAGG
ENST00000491673.1:n.361_370delinsCTGGACAAGG
ENST00000493253.5:n.82_91delinsCTGGACAAGG
ENST00000540235.5:c.71+19_72-15delinsCTGGACAAGG	ENSP00000441751.2:n.71+19_72-15delinsCTGGACAAGG
ENST00000577817.3:c.250_259delinsCTGGACAAGG	ENSP00000467418.1:p.Leu84=
NM_000422.2:c.295_304delinsCTGGACAAGG	NP_000413.1:p.Leu99=
NM_000422.3:c.295_304delinsCTGGACAAGG MANE Select	NP_000413.1:p.Leu99=