Canonical Allele Identifier: CA412892008

Gene: PQBP1

Linked Data

• MyVariant Identifiers: chrX:g.48760352G>C (hg19) ; chrX:g.48903075G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48903075G>C , CM000685.2:g.48903075G>C	GRCh38
NC_000023.10:g.48760352G>C , CM000685.1:g.48760352G>C	GRCh37
NC_000023.9:g.48645296G>C	NCBI36
NG_015967.1:g.10158G>C
NG_015968.2:g.75C>G
NG_034300.1:g.13884C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218224.9:c.789G>C	ENSP00000218224.4:p.Gln263His
ENST00000376563.6:c.789G>C	ENSP00000365747.1:p.Gln263His
ENST00000396763.6:c.789G>C	ENSP00000379985.1:p.Gln263His
ENST00000443648.6:c.789G>C	ENSP00000414861.2:p.Gln263His
ENST00000456306.2:c.180G>C	ENSP00000393013.2:p.Gln60His
ENST00000472742.6:c.*206G>C	ENSP00000509191.1:n.*206G>C
ENST00000474671.6:n.1944G>C
ENST00000477997.6:n.1738G>C
ENST00000486150.6:n.2044G>C
ENST00000692023.1:c.*1210G>C	ENSP00000509927.1:n.*1210G>C
ENST00000447146.7:c.789G>C MANE Select	ENSP00000391759.2:p.Gln263His
ENST00000651767.1:c.789G>C	ENSP00000498362.1:p.Gln263His
ENST00000218224.8:c.789G>C	ENSP00000218224.4:p.Gln263His
ENST00000247140.8:c.504G>C	ENSP00000247140.4:p.Gln168His
ENST00000376563.5:c.789G>C	ENSP00000365747.1:p.Gln263His
ENST00000376566.8:c.504G>C	ENSP00000365750.4:p.Gln168His
ENST00000396763.5:c.789G>C	ENSP00000379985.1:p.Gln263His
ENST00000447146.6:c.789G>C	ENSP00000391759.2:p.Gln263His
ENST00000463529.4:n.1135G>C
ENST00000465859.2:n.803G>C
ENST00000470059.5:n.1003G>C
ENST00000470062.5:n.761G>C
ENST00000473764.5:n.1361G>C
ENST00000474671.5:n.849G>C
ENST00000477997.5:n.870G>C
NM_001032381.1:c.789G>C	NP_001027553.1:p.Gln263His
NM_001032382.1:c.789G>C	NP_001027554.1:p.Gln263His
NM_001032383.1:c.789G>C	NP_001027555.1:p.Gln263His
NM_001032384.1:c.789G>C	NP_001027556.1:p.Gln263His
NM_001167989.1:c.786G>C	NP_001161461.1:p.Gln262His
NM_001167990.1:c.765G>C	NP_001161462.1:p.Gln255His
NM_001167992.1:c.489G>C	NP_001161464.1:p.Gln163His
NM_005710.2:c.789G>C	NP_005701.1:p.Gln263His
NM_144495.2:c.504G>C	NP_652766.1:p.Gln168His
XM_005272571.3:c.786G>C	XP_005272628.1:p.Gln262His
XM_005272572.3:c.504G>C	XP_005272629.1:p.Gln168His
XM_011543884.1:c.789G>C	XP_011542186.1:p.Gln263His
XM_005272572.4:c.504G>C	XP_005272629.1:p.Gln168His
XM_011543884.2:c.789G>C	XP_011542186.1:p.Gln263His
XM_017029207.1:c.786G>C	XP_016884696.1:p.Gln262His
NM_001032381.2:c.789G>C	NP_001027553.1:p.Gln263His
NM_001032382.2:c.789G>C MANE Select	NP_001027554.1:p.Gln263His
NM_001032383.2:c.789G>C	NP_001027555.1:p.Gln263His
NM_001167989.2:c.786G>C	NP_001161461.1:p.Gln262His
NM_001167990.2:c.765G>C	NP_001161462.1:p.Gln255His
NM_144495.3:c.504G>C	NP_652766.1:p.Gln168His