Canonical Allele Identifier: CA412891611

Gene: PQBP1

Linked Data

• MyVariant Identifiers: chrX:g.48760257G>C (hg19) ; chrX:g.48902980G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48902980G>C , CM000685.2:g.48902980G>C	GRCh38
NC_000023.10:g.48760257G>C , CM000685.1:g.48760257G>C	GRCh37
NC_000023.9:g.48645201G>C	NCBI36
NG_015967.1:g.10063G>C
NG_015968.2:g.170C>G
NG_034300.1:g.13979C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218224.9:c.694G>C	ENSP00000218224.4:p.Asp232His
ENST00000376563.6:c.694G>C	ENSP00000365747.1:p.Asp232His
ENST00000396763.6:c.694G>C	ENSP00000379985.1:p.Asp232His
ENST00000443648.6:c.694G>C	ENSP00000414861.2:p.Asp232His
ENST00000456306.2:c.85G>C	ENSP00000393013.2:p.Asp29His
ENST00000472742.6:c.*111G>C	ENSP00000509191.1:n.*111G>C
ENST00000474671.6:n.1849G>C
ENST00000477997.6:n.1643G>C
ENST00000486150.6:n.1949G>C
ENST00000692023.1:c.*1115G>C	ENSP00000509927.1:n.*1115G>C
ENST00000447146.7:c.694G>C MANE Select	ENSP00000391759.2:p.Asp232His
ENST00000651767.1:c.694G>C	ENSP00000498362.1:p.Asp232His
ENST00000218224.8:c.694G>C	ENSP00000218224.4:p.Asp232His
ENST00000247140.8:c.409G>C	ENSP00000247140.4:p.Asp137His
ENST00000376563.5:c.694G>C	ENSP00000365747.1:p.Asp232His
ENST00000376566.8:c.409G>C	ENSP00000365750.4:p.Asp137His
ENST00000396763.5:c.694G>C	ENSP00000379985.1:p.Asp232His
ENST00000447146.6:c.694G>C	ENSP00000391759.2:p.Asp232His
ENST00000456306.1:c.375G>C
ENST00000463529.4:n.1040G>C
ENST00000465859.2:n.708G>C
ENST00000470059.5:n.908G>C
ENST00000470062.5:n.666G>C
ENST00000473764.5:n.1266G>C
ENST00000474671.5:n.754G>C
ENST00000477997.5:n.775G>C
NM_001032381.1:c.694G>C	NP_001027553.1:p.Asp232His
NM_001032382.1:c.694G>C	NP_001027554.1:p.Asp232His
NM_001032383.1:c.694G>C	NP_001027555.1:p.Asp232His
NM_001032384.1:c.694G>C	NP_001027556.1:p.Asp232His
NM_001167989.1:c.691G>C	NP_001161461.1:p.Asp231His
NM_001167990.1:c.670G>C	NP_001161462.1:p.Asp224His
NM_001167992.1:c.394G>C	NP_001161464.1:p.Asp132His
NM_005710.2:c.694G>C	NP_005701.1:p.Asp232His
NM_144495.2:c.409G>C	NP_652766.1:p.Asp137His
XM_005272571.3:c.691G>C	XP_005272628.1:p.Asp231His
XM_005272572.3:c.409G>C	XP_005272629.1:p.Asp137His
XM_011543884.1:c.694G>C	XP_011542186.1:p.Asp232His
XM_005272572.4:c.409G>C	XP_005272629.1:p.Asp137His
XM_011543884.2:c.694G>C	XP_011542186.1:p.Asp232His
XM_017029207.1:c.691G>C	XP_016884696.1:p.Asp231His
NM_001032381.2:c.694G>C	NP_001027553.1:p.Asp232His
NM_001032382.2:c.694G>C MANE Select	NP_001027554.1:p.Asp232His
NM_001032383.2:c.694G>C	NP_001027555.1:p.Asp232His
NM_001167989.2:c.691G>C	NP_001161461.1:p.Asp231His
NM_001167990.2:c.670G>C	NP_001161462.1:p.Asp224His
NM_144495.3:c.409G>C	NP_652766.1:p.Asp137His