Canonical Allele Identifier: CA749314229

Gene: B3GALT5 IGSF5

Linked Data

• dbSNP Id: rs1201477033
• MyVariant Identifiers: chr21:g.41021537C>G (hg19) ; chr21:g.39649610C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.39649610C>G , CM000683.2:g.39649610C>G	GRCh38
NC_000021.8:g.41021537C>G , CM000683.1:g.41021537C>G	GRCh37
NC_000021.7:g.39943407C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343118.6:c.-161+7134C>G (B3GALT5)	ENSP00000343318.4:n.-161+7134C>G
ENST00000398714.4:c.-160-10143C>G (B3GALT5)	ENSP00000381699.4:n.-160-10143C>G
ENST00000615480.5:c.-160-10143C>G (B3GALT5)	ENSP00000480285.1:n.-160-10143C>G
ENST00000682542.1:c.-161+2988C>G (B3GALT5)	ENSP00000507453.1:n.-161+2988C>G
ENST00000682818.1:n.333+2988C>G (B3GALT5)
ENST00000683344.1:c.-161+2988C>G (B3GALT5)	ENSP00000508165.1:n.-161+2988C>G
ENST00000684187.2:c.-161+2988C>G (B3GALT5) MANE Select	ENSP00000506797.1:n.-161+2988C>G
ENST00000684495.1:c.-161+2988C>G (B3GALT5)	ENSP00000507285.1:n.-161+2988C>G
ENST00000380620.8:c.-161+2988C>G (B3GALT5)	ENSP00000369994.3:n.-161+2988C>G
ENST00000615480.4:c.-160-10143C>G (B3GALT5)	ENSP00000480285.1:n.-160-10143C>G
NM_001278650.1:c.-160-10143C>G (B3GALT5)	NP_001265579.1:n.-160-10143C>G
XR_937730.1:n.368-2964C>G
XR_937731.1:n.369-1303C>G
XR_937732.1:n.369-2967C>G
NM_001356336.1:c.-161+2988C>G (B3GALT5)	NP_001343265.1:n.-161+2988C>G
NM_001356338.1:c.-161+2988C>G (B3GALT5)	NP_001343267.1:n.-161+2988C>G
NM_001356339.1:c.-161+7134C>G (B3GALT5)	NP_001343268.1:n.-161+7134C>G
XM_011529472.2:c.-1107+17100C>G (IGSF5)	XP_011527774.1:n.-1107+17100C>G
NM_001356336.2:c.-161+2988C>G (B3GALT5) MANE Select	NP_001343265.1:n.-161+2988C>G
NM_001356338.2:c.-161+2988C>G (B3GALT5)	NP_001343267.1:n.-161+2988C>G
NM_001356339.2:c.-161+7134C>G (B3GALT5)	NP_001343268.1:n.-161+7134C>G
NM_001278650.2:c.-160-10143C>G (B3GALT5)	NP_001265579.1:n.-160-10143C>G