Canonical Allele Identifier: CA2693068845
Gene: GPR143 HGNC NCBI

Linked Data

dbSNP Id: rs1446155532
gnomAD v4: X-9741109-T-TA
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.9741116dup , CM000685.2:g.9741116dup GRCh38
NC_000023.10:g.9709156dup , CM000685.1:g.9709156dup GRCh37
NC_000023.9:g.9669156dup NCBI36
NG_009074.1:g.29768dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000467482.6:c.885+228dup MANE Select ENSP00000417161.1:n.885+228dup
ENST00000447366.5:c.633+228dup ENSP00000390546.2:n.633+228dup
ENST00000467482.5:c.885+228dup ENSP00000417161.1:n.885+228dup
NM_000273.2:c.885+228dup NP_000264.2:n.885+228dup
XM_005274541.2:c.885+228dup XP_005274598.1:n.885+228dup
XM_005274541.3:c.885+228dup XP_005274598.1:n.885+228dup
XM_024452387.1:c.633+228dup XP_024308155.1:n.633+228dup
XM_024452388.1:c.633+228dup XP_024308156.1:n.633+228dup
NM_000273.3:c.885+228dup MANE Select NP_000264.2:n.885+228dup
Search 100 bp 5'
Search 100 bp 3'