Canonical Allele Identifier: CA2243897135

Gene: ASPA SPATA22

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.3499005G= , CM000679.2:g.3499005G=	GRCh38
NC_000017.10:g.3402299G= , CM000679.1:g.3402299G=	GRCh37
NC_000017.9:g.3349049G=	NCBI36
NG_008399.1:g.29896G=
NG_008399.2:g.30360G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000049.4:c.859G= (ASPA) MANE Select	NP_000040.1:p.Ala287=
ENST00000263080.3:c.859G= (ASPA) MANE Select	ENSP00000263080.2:p.Ala287=
NM_000049.2:c.859G= (ASPA)	NP_000040.1:p.Ala287=
NM_000049.3:c.859G= (ASPA)	NP_000040.1:p.Ala287=
NM_001128085.1:c.859G= (ASPA)	NP_001121557.1:p.Ala287=
NM_001321336.1:c.-74+14407C= (SPATA22)	NP_001308265.1:n.-74+14407C=
NM_001321336.2:c.-74+14407C= (SPATA22)	NP_001308265.1:n.-74+14407C=
NM_001321337.1:c.-74+14407C= (SPATA22)	NP_001308266.1:n.-74+14407C=
NM_001321337.2:c.-74+14407C= (SPATA22)	NP_001308266.1:n.-74+14407C=
ENST00000263080.2:c.859G= (ASPA)	ENSP00000263080.2:p.Ala287=
ENST00000456349.6:c.859G= (ASPA)	ENSP00000409976.2:p.Ala287=
ENST00000541913.5:c.-74+14407C= (SPATA22)	ENSP00000441920.1:n.-74+14407C=
ENST00000570318.1:c.-74+14606C= (SPATA22)	ENSP00000459147.1:n.-74+14606C=
XM_005256829.1:c.-74+14407C= (SPATA22)	XP_005256886.1:n.-74+14407C=
XM_005256830.1:c.-74+14407C= (SPATA22)	XP_005256887.1:n.-74+14407C=
XM_006721527.2:c.859G= (ASPA)	XP_006721590.1:p.Ala287=
XM_017024661.1:c.859G= (ASPA)	XP_016880150.1:p.Ala287=
XM_024450764.1:c.859G= (ASPA)	XP_024306532.1:p.Ala287=
XR_934026.2:n.1126G= (ASPA)