Canonical Allele Identifier: CA703313

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.26318060G>C , CM000663.2:g.26318060G>C GRCh38
NC_000001.10:g.26644551G>C , CM000663.1:g.26644551G>C GRCh37
NC_000001.9:g.26517138G>C NCBI36
NG_028986.1:g.5206C>G

Transcript Alleles

HGVS Amino-acid Change
NM_001803.3:c.43G>C (CD52) MANE Select NP_001794.2:p.Val15Leu
ENST00000374213.3:c.43G>C (CD52) MANE Select ENSP00000363330.2:p.Val15Leu
NM_001803.2:c.43G>C (CD52) NP_001794.2:p.Val15Leu
NM_145345.2:c.-162C>G (UBXN11) NP_663320.2:n.-162C>G
NM_145345.3:c.-162C>G (UBXN11) NP_663320.2:n.-162C>G
ENST00000374213.2:c.43G>C (CD52) ENSP00000363330.2:p.Val15Leu
ENST00000374217.6:c.-162C>G (UBXN11) ENSP00000363334.2:n.-162C>G
ENST00000374217.7:c.-162C>G (UBXN11) ENSP00000363334.2:n.-162C>G
ENST00000374222.5:c.-162C>G (UBXN11) ENSP00000363339.1:n.-162C>G
ENST00000470468.1:n.103G>C (CD52)
ENST00000492808.5:n.103G>C (CD52)