Canonical Allele Identifier: CA226176
Gene: GPR143 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.9760704G>C , CM000685.2:g.9760704G>C GRCh38
NC_000023.10:g.9728744G>C , CM000685.1:g.9728744G>C GRCh37
NC_000023.9:g.9688744G>C NCBI36
NG_009074.1:g.10174C>G

Transcript Alleles

HGVS Amino-acid Change
NM_000273.3:c.360+13C>G MANE Select NP_000264.2:n.360+13C>G
ENST00000467482.6:c.360+13C>G MANE Select ENSP00000417161.1:n.360+13C>G
NM_000273.2:c.360+13C>G NP_000264.2:n.360+13C>G
ENST00000431126.1:c.108+13C>G ENSP00000406138.1:n.108+13C>G
ENST00000447366.5:c.108+13C>G ENSP00000390546.2:n.108+13C>G
ENST00000467482.5:c.360+13C>G ENSP00000417161.1:n.360+13C>G
XM_005274541.2:c.360+13C>G XP_005274598.1:n.360+13C>G
XM_005274541.3:c.360+13C>G XP_005274598.1:n.360+13C>G
XM_024452387.1:c.108+13C>G XP_024308155.1:n.108+13C>G
XM_024452388.1:c.108+13C>G XP_024308156.1:n.108+13C>G