Canonical Allele Identifier: CA2243897069
Gene: ASPA HGNC NCBI
SPATA22 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.3498980G= , CM000679.2:g.3498980G= GRCh38
NC_000017.10:g.3402274G= , CM000679.1:g.3402274G= GRCh37
NC_000017.9:g.3349024G= NCBI36
NG_008399.1:g.29871G=
NG_008399.2:g.30335G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263080.3:c.834G= (ASPA) MANE Select ENSP00000263080.2:p.Val278=
ENST00000263080.2:c.834G= (ASPA) ENSP00000263080.2:p.Val278=
ENST00000456349.6:c.834G= (ASPA) ENSP00000409976.2:p.Val278=
ENST00000541913.5:c.-74+14432C= (SPATA22) ENSP00000441920.1:n.-74+14432C=
ENST00000570318.1:c.-74+14631C= (SPATA22) ENSP00000459147.1:n.-74+14631C=
NM_000049.2:c.834G= (ASPA) NP_000040.1:p.Val278=
NM_001128085.1:c.834G= (ASPA) NP_001121557.1:p.Val278=
XM_005256829.1:c.-74+14432C= (SPATA22) XP_005256886.1:n.-74+14432C=
XM_005256830.1:c.-74+14432C= (SPATA22) XP_005256887.1:n.-74+14432C=
XM_006721527.2:c.834G= (ASPA) XP_006721590.1:p.Val278=
NM_001321336.1:c.-74+14432C= (SPATA22) NP_001308265.1:n.-74+14432C=
NM_001321337.1:c.-74+14432C= (SPATA22) NP_001308266.1:n.-74+14432C=
XM_017024661.1:c.834G= (ASPA) XP_016880150.1:p.Val278=
XM_024450764.1:c.834G= (ASPA) XP_024306532.1:p.Val278=
XR_934026.2:n.1101G= (ASPA)
NM_000049.3:c.834G= (ASPA) NP_000040.1:p.Val278=
NM_000049.4:c.834G= (ASPA) MANE Select NP_000040.1:p.Val278=
NM_001321336.2:c.-74+14432C= (SPATA22) NP_001308265.1:n.-74+14432C=
NM_001321337.2:c.-74+14432C= (SPATA22) NP_001308266.1:n.-74+14432C=