Canonical Allele Identifier: CA516031736

Gene: PQBP1

Linked Data

• MyVariant Identifiers: chrX:g.48760307A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48903030A>C , CM000685.2:g.48903030A>C	GRCh38
NC_000023.10:g.48760307A>C , CM000685.1:g.48760307A>C	GRCh37
NC_000023.9:g.48645251A>C	NCBI36
NG_015967.1:g.10113A>C
NG_015968.2:g.120T>G
NG_034300.1:g.13929T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218224.9:c.744A>C	ENSP00000218224.4:p.Pro248=
ENST00000376563.6:c.744A>C	ENSP00000365747.1:p.Pro248=
ENST00000396763.6:c.744A>C	ENSP00000379985.1:p.Pro248=
ENST00000443648.6:c.744A>C	ENSP00000414861.2:p.Pro248=
ENST00000456306.2:c.135A>C	ENSP00000393013.2:p.Pro45=
ENST00000472742.6:c.*161A>C	ENSP00000509191.1:n.*161A>C
ENST00000474671.6:n.1899A>C
ENST00000477997.6:n.1693A>C
ENST00000486150.6:n.1999A>C
ENST00000692023.1:c.*1165A>C	ENSP00000509927.1:n.*1165A>C
ENST00000447146.7:c.744A>C MANE Select	ENSP00000391759.2:p.Pro248=
ENST00000651767.1:c.744A>C	ENSP00000498362.1:p.Pro248=
ENST00000218224.8:c.744A>C	ENSP00000218224.4:p.Pro248=
ENST00000247140.8:c.459A>C	ENSP00000247140.4:p.Pro153=
ENST00000376563.5:c.744A>C	ENSP00000365747.1:p.Pro248=
ENST00000376566.8:c.459A>C	ENSP00000365750.4:p.Pro153=
ENST00000396763.5:c.744A>C	ENSP00000379985.1:p.Pro248=
ENST00000447146.6:c.744A>C	ENSP00000391759.2:p.Pro248=
ENST00000456306.1:c.425A>C
ENST00000463529.4:n.1090A>C
ENST00000465859.2:n.758A>C
ENST00000470059.5:n.958A>C
ENST00000470062.5:n.716A>C
ENST00000473764.5:n.1316A>C
ENST00000474671.5:n.804A>C
ENST00000477997.5:n.825A>C
NM_001032381.1:c.744A>C	NP_001027553.1:p.Pro248=
NM_001032382.1:c.744A>C	NP_001027554.1:p.Pro248=
NM_001032383.1:c.744A>C	NP_001027555.1:p.Pro248=
NM_001032384.1:c.744A>C	NP_001027556.1:p.Pro248=
NM_001167989.1:c.741A>C	NP_001161461.1:p.Pro247=
NM_001167990.1:c.720A>C	NP_001161462.1:p.Pro240=
NM_001167992.1:c.444A>C	NP_001161464.1:p.Pro148=
NM_005710.2:c.744A>C	NP_005701.1:p.Pro248=
NM_144495.2:c.459A>C	NP_652766.1:p.Pro153=
XM_005272571.3:c.741A>C	XP_005272628.1:p.Pro247=
XM_005272572.3:c.459A>C	XP_005272629.1:p.Pro153=
XM_011543884.1:c.744A>C	XP_011542186.1:p.Pro248=
XM_005272572.4:c.459A>C	XP_005272629.1:p.Pro153=
XM_011543884.2:c.744A>C	XP_011542186.1:p.Pro248=
XM_017029207.1:c.741A>C	XP_016884696.1:p.Pro247=
NM_001032381.2:c.744A>C	NP_001027553.1:p.Pro248=
NM_001032382.2:c.744A>C MANE Select	NP_001027554.1:p.Pro248=
NM_001032383.2:c.744A>C	NP_001027555.1:p.Pro248=
NM_001167989.2:c.741A>C	NP_001161461.1:p.Pro247=
NM_001167990.2:c.720A>C	NP_001161462.1:p.Pro240=
NM_144495.3:c.459A>C	NP_652766.1:p.Pro153=