Canonical Allele Identifier: CA2637840912

Gene: KRT17

Linked Data

• gnomAD v4: 17-41624513-G-GA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624513_41624514insA , CM000679.2:g.41624513_41624514insA	GRCh38
NC_000017.10:g.39780765_39780766insA , CM000679.1:g.39780765_39780766insA	GRCh37
NC_000017.9:g.37034291_37034292insA	NCBI36
NG_008625.1:g.5117_5118insT
NG_009090.2:g.167199_167200insT , LRG_401:g.167199_167200insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.-5_-4insT MANE Select	ENSP00000308452.8:n.-5_-4insT
ENST00000311208.12:c.-5_-4insT	ENSP00000308452.8:n.-5_-4insT
ENST00000463128.5:c.-313+229_-313+230insT	ENSP00000468672.1:n.-313+229_-313+230insT
ENST00000491673.1:n.62_63insT
ENST00000540235.5:c.-210_-209insT	ENSP00000441751.2:n.-210_-209insT
NM_000422.2:c.-5_-4insT	NP_000413.1:n.-5_-4insT
NM_000422.3:c.-5_-4insT MANE Select	NP_000413.1:n.-5_-4insT