Canonical Allele Identifier: CA2695225892
Gene: KRT17 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41624232_41624241delinsA , CM000679.2:g.41624232_41624241delinsA GRCh38
NC_000017.10:g.39780484_39780493delinsA , CM000679.1:g.39780484_39780493delinsA GRCh37
NC_000017.9:g.37034010_37034019delinsA NCBI36
NG_008625.1:g.5390_5399delinsT
NG_009090.2:g.167472_167481delinsT , LRG_401:g.167472_167481delinsT

Transcript Alleles

HGVS Amino-acid change
ENST00000311208.13:c.269_278delinsT MANE Select ENSP00000308452.8:p.Asn90_Asp93delinsIle
ENST00000311208.12:c.269_278delinsT ENSP00000308452.8:p.Asn90_Asp93delinsIle
ENST00000463128.5:c.-312-35_-312-26delinsT ENSP00000468672.1:n.-312-35_-312-26delins...
ENST00000491673.1:n.335_344delinsT
ENST00000493253.5:n.56_65delinsT
ENST00000540235.5:c.64_71+2delinsT
ENST00000577817.3:c.224_233delinsT ENSP00000467418.1:p.Asn75_Asp78delinsIle
NM_000422.2:c.269_278delinsT NP_000413.1:p.Asn90_Asp93delinsIle
NM_000422.3:c.269_278delinsT MANE Select NP_000413.1:p.Asn90_Asp93delinsIle