Canonical Allele Identifier: CA1872987347

Gene: KIAA1958

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.112519756T= , CM000671.2:g.112519756T=	GRCh38
NC_000009.11:g.115282036T= , CM000671.1:g.115282036T=	GRCh37
NC_000009.10:g.114321857T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_133465.4:c.-25+32638T= MANE Select	NP_597722.1:n.-25+32638T=
ENST00000337530.11:c.-25+32638T= MANE Select	ENSP00000336940.6:n.-25+32638T=
NM_001287036.1:c.-25+32638T=	NP_001273965.1:n.-25+32638T=
NM_001287036.2:c.-25+32638T=	NP_001273965.1:n.-25+32638T=
NM_001287038.1:c.-25+32638T=	NP_001273967.1:n.-25+32638T=
NM_001287038.2:c.-25+32638T=	NP_001273967.1:n.-25+32638T=
NM_133465.3:c.-25+32638T=	NP_597722.1:n.-25+32638T=
ENST00000337530.10:c.-25+32638T=	ENSP00000336940.6:n.-25+32638T=
ENST00000374244.3:c.-25+32638T=	ENSP00000363362.3:n.-25+32638T=
ENST00000536272.5:c.-25+32638T=	ENSP00000440504.1:n.-25+32638T=
XM_006716978.2:c.-25+32638T=	XP_006717041.1:n.-25+32638T=
XM_011518310.1:c.-25+32638T=	XP_011516612.1:n.-25+32638T=