Canonical Allele Identifier: CA2637840893

Gene: KRT17

Linked Data

• gnomAD v4: 17-41624275-G-GCCCATCAA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624277_41624284dup , CM000679.2:g.41624277_41624284dup	GRCh38
NC_000017.10:g.39780529_39780536dup , CM000679.1:g.39780529_39780536dup	GRCh37
NC_000017.9:g.37034055_37034062dup	NCBI36
NG_008625.1:g.5348_5355dup
NG_009090.2:g.167430_167437dup , LRG_401:g.167430_167437dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.227_234dup MANE Select	ENSP00000308452.8:p.Leu80MetfsTer?
ENST00000311208.12:c.227_234dup	ENSP00000308452.8:p.Leu80MetfsTer?
ENST00000463128.5:c.-312-77_-312-70dup	ENSP00000468672.1:n.-312-77_-312-70dup
ENST00000491673.1:n.293_300dup
ENST00000493253.5:n.14_21dup
ENST00000540235.5:c.22_29dup	ENSP00000441751.2:p.Cys11Ter
ENST00000577817.3:c.182_189dup	ENSP00000467418.1:p.Leu65MetfsTer?
NM_000422.2:c.227_234dup	NP_000413.1:p.Leu80MetfsTer?
NM_000422.3:c.227_234dup MANE Select	NP_000413.1:p.Leu80MetfsTer?