Canonical Allele Identifier: CA1624357146

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.43047995_43047996delinsTA , CM000668.2:g.43047995_43047996delinsTA GRCh38
NC_000006.11:g.43015733_43015734delinsTA , CM000668.1:g.43015733_43015734delinsTA GRCh37
NC_000006.10:g.43123711_43123712delinsTA NCBI36
NG_016205.1:g.10950_10951delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000478630.2:n.14-7_14-6delinsTA (CUL7)
ENST00000674112.2:c.2169+152_2169+153delinsTA (CUL7) ENSP00000501166.2:n.2169+152_2169+153delinsTA
ENST00000685042.1:c.2169+152_2169+153delinsTA (CUL7) ENSP00000509871.1:n.2169+152_2169+153delinsTA
ENST00000686442.1:n.2452+152_2452+153delinsTA (CUL7)
ENST00000687225.1:c.2266-7_2266-6delinsTA (CUL7) ENSP00000509364.1:n.2266-7_2266-6delinsTA
ENST00000688302.1:n.2452+152_2452+153delinsTA (CUL7)
ENST00000689256.1:n.2468+152_2468+153delinsTA (CUL7)
ENST00000690231.1:c.2169+152_2169+153delinsTA (CUL7) ENSP00000508461.1:n.2169+152_2169+153delinsTA
ENST00000265348.9:c.2169+152_2169+153delinsTA (CUL7) MANE Select ENSP00000265348.4:n.2169+152_2169+153delinsTA
ENST00000673725.1:c.118+152_118+153delinsTA (CUL7)
ENST00000673753.1:n.2504-7_2504-6delinsTA (CUL7)
ENST00000674100.1:c.2265+152_2265+153delinsTA (CUL7) ENSP00000501292.1:n.2265+152_2265+153delinsTA
ENST00000674112.1:c.661+152_661+153delinsTA (CUL7)
ENST00000674134.1:c.2265+152_2265+153delinsTA (CUL7) ENSP00000501068.1:n.2265+152_2265+153delinsTA
ENST00000265348.7:c.2169+152_2169+153delinsTA (CUL7) ENSP00000265348.3:n.2169+152_2169+153delinsTA
ENST00000467906.5:c.-553+4487_-553+4488delinsTA (KLC4) ENSP00000418759.1:n.-553+4487_-553+4488delinsTA
ENST00000478630.1:n.14-7_14-6delinsTA (CUL7)
ENST00000535468.1:c.2421+152_2421+153delinsTA (CUL7) ENSP00000438788.1:n.2421+152_2421+153delinsTA
NM_001168370.1:c.2421+152_2421+153delinsTA (CUL7) NP_001161842.1:n.2421+152_2421+153delinsTA
NM_014780.4:c.2169+152_2169+153delinsTA (CUL7) NP_055595.2:n.2169+152_2169+153delinsTA
XM_005249503.1:c.2325+152_2325+153delinsTA (CUL7) XP_005249560.1:n.2325+152_2325+153delinsTA
XM_006715285.1:c.2265+152_2265+153delinsTA (CUL7) XP_006715348.1:n.2265+152_2265+153delinsTA
XM_011515019.1:c.2421+152_2421+153delinsTA (CUL7) XP_011513321.1:n.2421+152_2421+153delinsTA
XM_011515020.1:c.2325+152_2325+153delinsTA (CUL7) XP_011513322.1:n.2325+152_2325+153delinsTA
XM_011515021.1:c.-13-7_-13-6delinsTA (CUL7) XP_011513323.1:n.-13-7_-13-6delinsTA
XM_005249503.3:c.2325+152_2325+153delinsTA (CUL7) XP_005249560.1:n.2325+152_2325+153delinsTA
XM_006715285.2:c.2265+152_2265+153delinsTA (CUL7) XP_006715348.1:n.2265+152_2265+153delinsTA
XM_011515019.2:c.2421+152_2421+153delinsTA (CUL7) XP_011513321.1:n.2421+152_2421+153delinsTA
XM_011515020.2:c.2325+152_2325+153delinsTA (CUL7) XP_011513322.1:n.2325+152_2325+153delinsTA
XM_017011533.1:c.2448+152_2448+153delinsTA (CUL7) XP_016867022.1:n.2448+152_2448+153delinsTA
XM_017011534.1:c.2448+152_2448+153delinsTA (CUL7) XP_016867023.1:n.2448+152_2448+153delinsTA
XM_017011535.1:c.2352+152_2352+153delinsTA (CUL7) XP_016867024.1:n.2352+152_2352+153delinsTA
XM_017011536.2:c.2292+152_2292+153delinsTA (CUL7) XP_016867025.1:n.2292+152_2292+153delinsTA
XM_017011537.2:c.2265+152_2265+153delinsTA (CUL7) XP_016867026.1:n.2265+152_2265+153delinsTA
XM_017011538.2:c.2196+152_2196+153delinsTA (CUL7) XP_016867027.1:n.2196+152_2196+153delinsTA
XM_017011539.2:c.2169+152_2169+153delinsTA (CUL7) XP_016867028.1:n.2169+152_2169+153delinsTA
XM_017011540.1:c.2448+152_2448+153delinsTA (CUL7) XP_016867029.1:n.2448+152_2448+153delinsTA
NM_001168370.2:c.2265+152_2265+153delinsTA (CUL7) NP_001161842.2:n.2265+152_2265+153delinsTA
NM_001374872.1:c.2265+152_2265+153delinsTA (CUL7) NP_001361801.1:n.2265+152_2265+153delinsTA
NM_001374873.1:c.2169+152_2169+153delinsTA (CUL7) NP_001361802.1:n.2169+152_2169+153delinsTA
NM_001374874.1:c.2169+152_2169+153delinsTA (CUL7) NP_001361803.1:n.2169+152_2169+153delinsTA
NM_014780.5:c.2169+152_2169+153delinsTA (CUL7) MANE Select NP_055595.2:n.2169+152_2169+153delinsTA