Canonical Allele Identifier: CA835210600

Gene: GIMAP5 GIMAP1-GIMAP5

Linked Data

• dbSNP Id: rs6598
• gnomAD v3: 7-150743561-G-C
• gnomAD v4: 7-150743561-G-C
• MyVariant Identifiers: chr7:g.150440649G>C (hg19) ; chr7:g.150743561G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150743561G>C , CM000669.2:g.150743561G>C	GRCh38
NC_000007.13:g.150440649G>C , CM000669.1:g.150440649G>C	GRCh37
NC_000007.12:g.150071582G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000358647.5:c.*498G>C (GIMAP5) MANE Select	ENSP00000351473.3:n.*498G>C
ENST00000358647.4:c.*498G>C (GIMAP5)	ENSP00000351473.3:n.*498G>C
ENST00000466347.5:n.131+2634G>C (GIMAP5)
ENST00000476324.1:n.4697G>C (GIMAP5)
ENST00000479556.1:n.1470G>C (GIMAP5)
ENST00000498181.6:c.*498G>C (GIMAP5)	ENSP00000487840.2:n.*498G>C
ENST00000611999.4:c.*498G>C (GIMAP1-GIMAP5)	ENSP00000477920.1:n.*498G>C
NM_001199577.1:c.*498G>C (GIMAP1-GIMAP5)	NP_001186506.1:n.*498G>C
NM_001303630.1:c.*498G>C (GIMAP1-GIMAP5)	NP_001290559.1:n.*498G>C
NM_018384.4:c.*498G>C (GIMAP5)	NP_060854.2:n.*498G>C
NM_001199577.2:c.*498G>C (GIMAP1-GIMAP5)	NP_001186506.1:n.*498G>C
NM_001303630.2:c.*498G>C (GIMAP1-GIMAP5)	NP_001290559.1:n.*498G>C
NM_018384.5:c.*498G>C (GIMAP5) MANE Select	NP_060854.2:n.*498G>C