Canonical Allele Identifier: CA1339206276
Gene: GPR35 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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