Canonical Allele Identifier: CA15776478
Gene: GPR183 HGNC NCBI
UBAC2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.99304368T>C , CM000675.2:g.99304368T>C GRCh38
NC_000013.10:g.99956622T>C , CM000675.1:g.99956622T>C GRCh37
NC_000013.9:g.98754623T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376414.5:c.-19+2972A>G (GPR183) MANE Select ENSP00000365596.4:n.-19+2972A>G
ENST00000403766.8:c.390-9729T>C (UBAC2) MANE Select ENSP00000383911.3:n.390-9729T>C
ENST00000355700.9:c.160-35952T>C (UBAC2) ENSP00000347928.5:n.160-35952T>C
ENST00000376414.4:c.-19+2972A>G (GPR183) ENSP00000365596.4:n.-19+2972A>G
ENST00000376440.6:c.285-9729T>C (UBAC2) ENSP00000365623.2:n.285-9729T>C
ENST00000403766.7:c.390-9729T>C (UBAC2) ENSP00000383911.3:n.390-9729T>C
ENST00000468067.5:n.551-9729T>C (UBAC2)
ENST00000473091.5:n.487-9729T>C (UBAC2)
ENST00000494576.5:n.111-9729T>C (UBAC2)
NM_001144072.1:c.390-9729T>C (UBAC2) NP_001137544.1:n.390-9729T>C
NM_004951.4:c.-19+2972A>G (GPR183) NP_004942.1:n.-19+2972A>G
NM_177967.3:c.285-9729T>C (UBAC2) NP_808882.1:n.285-9729T>C
NR_026644.1:n.1018-9729T>C (UBAC2)
XM_006719947.1:c.390-9729T>C (UBAC2) XP_006720010.1:n.390-9729T>C
XM_006719948.2:c.51-9729T>C (UBAC2) XP_006720011.1:n.51-9729T>C
XM_011521082.1:c.309-9729T>C (UBAC2) XP_011519384.1:n.309-9729T>C
XM_011521083.1:c.234-9729T>C (UBAC2) XP_011519385.1:n.234-9729T>C
XM_011521084.1:c.51-9729T>C (UBAC2) XP_011519386.1:n.51-9729T>C
XR_931613.1:n.519-9729T>C (UBAC2)
XM_006719948.3:c.51-9729T>C (UBAC2) XP_006720011.1:n.51-9729T>C
XM_011521082.2:c.309-9729T>C (UBAC2) XP_011519384.1:n.309-9729T>C
XM_011521083.2:c.234-9729T>C (UBAC2) XP_011519385.1:n.234-9729T>C
NM_004951.5:c.-19+2972A>G (GPR183) MANE Select NP_004942.1:n.-19+2972A>G
NM_001144072.2:c.390-9729T>C (UBAC2) MANE Select NP_001137544.1:n.390-9729T>C
NM_177967.4:c.285-9729T>C (UBAC2) NP_808882.1:n.285-9729T>C
NR_026644.2:n.1073-9729T>C (UBAC2)
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