Canonical Allele Identifier: CA2637840872

Gene: KRT17

Linked Data

• gnomAD v4: 17-41624043-GCCCCCCGGAGAC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624047_41624058del , CM000679.2:g.41624047_41624058del	GRCh38
NC_000017.10:g.39780299_39780310del , CM000679.1:g.39780299_39780310del	GRCh37
NC_000017.9:g.37033825_37033836del	NCBI36
NG_008625.1:g.5576_5587del
NG_009090.2:g.167658_167669del , LRG_401:g.167658_167669del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.432+23_432+34del MANE Select	ENSP00000308452.8:n.432+23_432+34del
ENST00000311208.12:c.432+23_432+34del	ENSP00000308452.8:n.432+23_432+34del
ENST00000463128.5:c.-184+23_-184+34del	ENSP00000468672.1:n.-184+23_-184+34del
ENST00000491673.1:n.498+23_498+34del
ENST00000493253.5:n.219+23_219+34del
ENST00000540235.5:c.183+23_183+34del	ENSP00000441751.2:n.183+23_183+34del
ENST00000577817.3:c.387+23_387+34del	ENSP00000467418.1:n.387+23_387+34del
NM_000422.2:c.432+23_432+34del	NP_000413.1:n.432+23_432+34del
NM_000422.3:c.432+23_432+34del MANE Select	NP_000413.1:n.432+23_432+34del