Canonical Allele Identifier: CA411999290

Gene: GPR143

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9760811G>T , CM000685.2:g.9760811G>T	GRCh38
NC_000023.10:g.9728851G>T , CM000685.1:g.9728851G>T	GRCh37
NC_000023.9:g.9688851G>T	NCBI36
NG_009074.1:g.10067C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000273.3:c.266C>A MANE Select	NP_000264.2:p.Ser89Tyr
ENST00000467482.6:c.266C>A MANE Select	ENSP00000417161.1:p.Ser89Tyr
NM_000273.2:c.266C>A	NP_000264.2:p.Ser89Tyr
ENST00000431126.1:c.14C>A	ENSP00000406138.1:p.Ser5Tyr
ENST00000447366.5:c.14C>A	ENSP00000390546.2:p.Ser5Tyr
ENST00000467482.5:c.266C>A	ENSP00000417161.1:p.Ser89Tyr
XM_005274541.2:c.266C>A	XP_005274598.1:p.Ser89Tyr
XM_005274541.3:c.266C>A	XP_005274598.1:p.Ser89Tyr
XM_024452387.1:c.14C>A	XP_024308155.1:p.Ser5Tyr
XM_024452388.1:c.14C>A	XP_024308156.1:p.Ser5Tyr