Canonical Allele Identifier: CA11053030

Gene: GPR35

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240624322G>A , CM000664.2:g.240624322G>A	GRCh38
NC_000002.11:g.241563739G>A , CM000664.1:g.241563739G>A	GRCh37
NC_000002.10:g.241212412G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319838.10:c.-5+5291G>A	ENSP00000322731.5:n.-5+5291G>A
ENST00000319838.9:c.-5+5291G>A	ENSP00000322731.5:n.-5+5291G>A
ENST00000403859.1:c.-5+5291G>A	ENSP00000385140.1:n.-5+5291G>A
ENST00000430267.2:c.89+5291G>A	ENSP00000411788.2:n.89+5291G>A
NM_001195381.1:c.89+5291G>A	NP_001182310.1:n.89+5291G>A
NM_001195382.1:c.89+5291G>A	NP_001182311.1:n.89+5291G>A
NM_001195381.2:c.89+5291G>A	NP_001182310.1:n.89+5291G>A
NM_001195382.2:c.89+5291G>A	NP_001182311.1:n.89+5291G>A
NM_001195381.3:c.89+5291G>A	NP_001182310.1:n.89+5291G>A
NM_001195382.3:c.89+5291G>A	NP_001182311.1:n.89+5291G>A
NM_001394730.1:c.89+5291G>A	NP_001381659.1:n.89+5291G>A