Canonical Allele Identifier: CA1208485286
Gene: KIAA0040 HGNC NCBI

Linked Data

dbSNP Id: rs1677458865

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.175181990C>A , CM000663.2:g.175181990C>A GRCh38
NC_000001.10:g.175151126C>A , CM000663.1:g.175151126C>A GRCh37
NC_000001.9:g.173417749C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000423313.6:c.-383-4306G>T MANE Select ENSP00000462172.1:n.-383-4306G>T
ENST00000423313.5:c.-383-4306G>T ENSP00000462172.1:n.-383-4306G>T
ENST00000444639.5:c.-383-4306G>T ENSP00000463734.1:n.-383-4306G>T
ENST00000545251.6:c.-310+10650G>T ENSP00000464040.1:n.-310+10650G>T
ENST00000563563.2:n.218-4306G>T
ENST00000567124.5:n.137-4306G>T
NM_001162893.1:c.-383-4306G>T NP_001156365.1:n.-383-4306G>T
NM_001162894.1:c.-383-4306G>T NP_001156366.1:n.-383-4306G>T
NM_001162895.1:c.-310+10650G>T NP_001156367.1:n.-310+10650G>T
NM_014656.2:c.-383-4306G>T NP_055471.2:n.-383-4306G>T
XM_005245628.3:c.-310+10870G>T XP_005245685.1:n.-310+10870G>T
XM_011510182.1:c.-766-4306G>T XP_011508484.1:n.-766-4306G>T
XM_011510183.1:c.-841-4306G>T XP_011508485.1:n.-841-4306G>T
XM_011510184.1:c.-458-4306G>T XP_011508486.1:n.-458-4306G>T
NM_001319230.1:c.-310+10870G>T NP_001306159.1:n.-310+10870G>T
NM_001319231.1:c.-458-4306G>T NP_001306160.1:n.-458-4306G>T
XM_017002911.2:c.-310+10650G>T XP_016858400.1:n.-310+10650G>T
NM_014656.3:c.-383-4306G>T MANE Select NP_055471.2:n.-383-4306G>T
NM_001162893.2:c.-383-4306G>T NP_001156365.1:n.-383-4306G>T
NM_001162894.2:c.-383-4306G>T NP_001156366.1:n.-383-4306G>T
NM_001162895.2:c.-310+10650G>T NP_001156367.1:n.-310+10650G>T
NM_001319230.2:c.-310+10870G>T NP_001306159.1:n.-310+10870G>T
NM_001319231.2:c.-458-4306G>T NP_001306160.1:n.-458-4306G>T