Canonical Allele Identifier: CA2415032259
Gene: GPR143 HGNC NCBI

Linked Data

dbSNP Id: rs2083523786
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.9765129C>T , CM000685.2:g.9765129C>T GRCh38
NC_000023.10:g.9733169C>T , CM000685.1:g.9733169C>T GRCh37
NC_000023.9:g.9693169C>T NCBI36
NG_009074.1:g.5749G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000467482.6:c.250+439G>A MANE Select ENSP00000417161.1:n.250+439G>A
ENST00000431126.1:c.-3+991G>A ENSP00000406138.1:n.-3+991G>A
ENST00000447366.5:c.-2-4303G>A ENSP00000390546.2:n.-2-4303G>A
ENST00000467482.5:c.250+439G>A ENSP00000417161.1:n.250+439G>A
NM_000273.2:c.250+439G>A NP_000264.2:n.250+439G>A
XM_005274541.2:c.250+439G>A XP_005274598.1:n.250+439G>A
XM_005274541.3:c.250+439G>A XP_005274598.1:n.250+439G>A
XM_024452387.1:c.-2-4303G>A XP_024308155.1:n.-2-4303G>A
XM_024452388.1:c.-2-4303G>A XP_024308156.1:n.-2-4303G>A
NM_000273.3:c.250+439G>A MANE Select NP_000264.2:n.250+439G>A
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