Canonical Allele Identifier: CA123332077

Gene: KIAA0825

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.94221997A>G , CM000667.2:g.94221997A>G	GRCh38
NC_000005.9:g.93557702A>G , CM000667.1:g.93557702A>G	GRCh37
NC_000005.8:g.93583458A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703867.1:c.3726-67873T>C	ENSP00000515512.1:n.3726-67873T>C
ENST00000682413.1:c.3711-67873T>C MANE Select	ENSP00000506760.1:n.3711-67873T>C
ENST00000513200.7:c.3711-67873T>C	ENSP00000424618.2:n.3711-67873T>C
NM_001145678.1:c.3711-67873T>C	NP_001139150.1:n.3711-67873T>C
XM_006714588.1:c.3726-67873T>C	XP_006714651.1:n.3726-67873T>C
XR_948247.1:n.4155-67873T>C
XR_948580.1:n.902+4536A>G
XR_948581.1:n.902+4536A>G
XR_948583.1:n.368+4536A>G
XM_006714588.2:c.3726-67873T>C	XP_006714651.1:n.3726-67873T>C
XR_001742440.1:n.938+4536A>G
XR_001742441.1:n.361+4536A>G
XR_001742442.1:n.320+4536A>G
XR_001742443.1:n.320+4536A>G
XR_948580.2:n.876+4536A>G
XR_948581.2:n.876+4536A>G
NM_001145678.2:c.3711-67873T>C	NP_001139150.1:n.3711-67873T>C
NM_001145678.3:c.3711-67873T>C MANE Select	NP_001139150.1:n.3711-67873T>C
NM_001385712.1:c.3726-67873T>C	NP_001372641.1:n.3726-67873T>C
NM_001388325.1:c.3726-67873T>C	NP_001375254.1:n.3726-67873T>C