Canonical Allele Identifier: CA626215611

Gene: KRT17

Linked Data

• dbSNP Id: rs1366592029
• gnomAD v2: 17-39780574-AAGCTGTAGC-A
• gnomAD v3: 17-41624322-AAGCTGTAGC-A
• gnomAD v4: 17-41624322-AAGCTGTAGC-A
• MyVariant Identifiers: chr17:g.39780575_39780583del (hg19) ; chr17:g.41624323_41624331del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41624328_41624336del , CM000679.2:g.41624328_41624336del	GRCh38
NC_000017.10:g.39780580_39780588del , CM000679.1:g.39780580_39780588del	GRCh37
NC_000017.9:g.37034106_37034114del	NCBI36
NG_008625.1:g.5300_5308del
NG_009090.2:g.167382_167390del , LRG_401:g.167382_167390del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311208.13:c.179_187del MANE Select	ENSP00000308452.8:p.Cys60_Ser62del
ENST00000311208.12:c.179_187del	ENSP00000308452.8:p.Cys60_Ser62del
ENST00000463128.5:c.-312-125_-312-117del	ENSP00000468672.1:n.-312-125_-312-117del
ENST00000491673.1:n.245_253del
ENST00000540235.5:c.-27_-19del	ENSP00000441751.2:n.-27_-19del
ENST00000577817.3:c.134_142del	ENSP00000467418.1:p.Cys45_Ser47del
NM_000422.2:c.179_187del	NP_000413.1:p.Cys60_Ser62del
NM_000422.3:c.179_187del MANE Select	NP_000413.1:p.Cys60_Ser62del