Canonical Allele Identifier: CA10623983
Community Standard Title: NC_000006.12:g.43053913C>G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.43053913C>G , CM000668.2:g.43053913C>G GRCh38
NC_000006.11:g.43021651C>G , CM000668.1:g.43021651C>G GRCh37
NC_000006.10:g.43129629C>G NCBI36
NG_016205.1:g.5033G>C

Transcript Alleles

HGVS Amino-acid Change
NM_001168370.1:c.-55G>C (CUL7) NP_001161842.1:n.-55G>C
NM_014780.4:c.-300G>C (CUL7) NP_055595.2:n.-300G>C
ENST00000467906.5:c.-552-5113C>G (KLC4) ENSP00000418759.1:n.-552-5113C>G
ENST00000535468.1:c.-55G>C (CUL7) ENSP00000438788.1:n.-55G>C
ENST00000673761.1:c.633+502G>C ENSP00000501018.1:n.633+502G>C
ENST00000674100.1:c.-300G>C (CUL7) ENSP00000501292.1:n.-300G>C
XM_006715285.1:c.-300G>C (CUL7) XP_006715348.1:n.-300G>C
XM_006715285.2:c.-300G>C (CUL7) XP_006715348.1:n.-300G>C
XM_017011536.2:c.-300G>C (CUL7) XP_016867025.1:n.-300G>C
XM_017011537.2:c.-300G>C (CUL7) XP_016867026.1:n.-300G>C
XM_017011538.2:c.-300G>C (CUL7) XP_016867027.1:n.-300G>C
XM_017011539.2:c.-300G>C (CUL7) XP_016867028.1:n.-300G>C