Canonical Allele Identifier: CA2073055433

Gene: GOLGA3

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.132769223C>G , CM000674.2:g.132769223C>G	GRCh38
NC_000012.11:g.133345809C>G , CM000674.1:g.133345809C>G	GRCh37
NC_000012.10:g.131855882C>G	NCBI36
NG_029887.1:g.64618G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000204726.9:c.*3882G>C	ENSP00000204726.3:n.*3882G>C
ENST00000450791.8:c.*3882G>C MANE Select	ENSP00000410378.2:n.*3882G>C
ENST00000687190.1:c.5090G>C	ENSP00000508882.1:n.5090G>C
ENST00000688114.1:c.*3882G>C	ENSP00000510765.1:n.*3882G>C
ENST00000690057.1:n.2383G>C
ENST00000690511.1:c.5692G>C	ENSP00000508770.1:n.5692G>C
ENST00000693666.1:c.7856G>C	ENSP00000509929.1:n.7856G>C
ENST00000204726.8:c.*3882G>C	ENSP00000204726.3:n.*3882G>C
ENST00000450791.7:c.*3882G>C	ENSP00000410378.2:n.*3882G>C
ENST00000204726.7:c.*3882G>C	ENSP00000204726.3:n.*3882G>C
ENST00000450791.6:c.*3882G>C	ENSP00000410378.2:n.*3882G>C
NM_005895.3:c.*3882G>C	NP_005886.2:n.*3882G>C
XM_005266162.2:c.*3882G>C	XP_005266219.1:n.*3882G>C
XM_005266164.3:c.*3882G>C	XP_005266221.1:n.*3882G>C
XM_005266165.3:c.*3882G>C	XP_005266222.1:n.*3882G>C
XM_005266167.3:c.*3882G>C	XP_005266224.1:n.*3882G>C
XM_006719736.2:c.*3882G>C	XP_006719799.1:n.*3882G>C
XM_006719737.2:c.*3882G>C	XP_006719800.1:n.*3882G>C
XM_006719738.2:c.*3882G>C	XP_006719801.1:n.*3882G>C
XM_011534790.1:c.*3882G>C	XP_011533092.1:n.*3882G>C
XM_011534791.1:c.*3882G>C	XP_011533093.1:n.*3882G>C
XM_011534792.1:c.*3882G>C	XP_011533094.1:n.*3882G>C
XM_011534793.1:c.*3882G>C	XP_011533095.1:n.*3882G>C
XM_011534794.1:c.*3882G>C	XP_011533096.1:n.*3882G>C
XM_005266164.4:c.*3882G>C	XP_005266221.1:n.*3882G>C
XM_005266167.4:c.*3882G>C	XP_005266224.1:n.*3882G>C
XM_006719736.3:c.*3882G>C	XP_006719799.1:n.*3882G>C
XM_006719737.3:c.*3882G>C	XP_006719800.1:n.*3882G>C
XM_011534793.2:c.*3882G>C	XP_011533095.1:n.*3882G>C
XM_011534794.2:c.*3882G>C	XP_011533096.1:n.*3882G>C
XM_024448939.1:c.*3882G>C	XP_024304707.1:n.*3882G>C
XM_024448940.1:c.*3882G>C	XP_024304708.1:n.*3882G>C
XM_024448941.1:c.*3882G>C	XP_024304709.1:n.*3882G>C
XM_024448942.1:c.*3882G>C	XP_024304710.1:n.*3882G>C
XM_024448943.1:c.*3882G>C	XP_024304711.1:n.*3882G>C
NM_005895.4:c.*3882G>C	NP_005886.2:n.*3882G>C
NM_001389683.1:c.*3882G>C MANE Select	NP_001376612.1:n.*3882G>C
NM_001389684.1:c.*3882G>C	NP_001376613.1:n.*3882G>C
NM_001389685.1:c.*3882G>C	NP_001376614.1:n.*3882G>C
NM_001389686.1:c.*3882G>C	NP_001376615.1:n.*3882G>C
NM_001389687.1:c.*3882G>C	NP_001376616.1:n.*3882G>C
NM_001389688.1:c.*3882G>C	NP_001376617.1:n.*3882G>C
NM_001389689.1:c.*3882G>C	NP_001376618.1:n.*3882G>C