Canonical Allele Identifier: CA658798676
Gene: ASPA HGNC NCBI
SPATA22 HGNC NCBI

Linked Data

ClinVar Variation Id: 523964
ClinVar RCV Id: RCV000627455
dbSNP Id: rs1555540679

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.3494404_3494413del , CM000679.2:g.3494404_3494413del GRCh38
NC_000017.10:g.3397698_3397707del , CM000679.1:g.3397698_3397707del GRCh37
NC_000017.9:g.3344448_3344457del NCBI36
NG_008399.1:g.25295_25304del
NG_008399.2:g.25759_25768del

Transcript Alleles

HGVS Amino-acid change
ENST00000263080.3:c.689_698del (ASPA) MANE Select ENSP00000263080.2:p.Asp230GlyfsTer?
ENST00000263080.2:c.689_698del (ASPA) ENSP00000263080.2:p.Asp230GlyfsTer?
ENST00000456349.6:c.689_698del (ASPA) ENSP00000409976.2:p.Asp230GlyfsTer?
ENST00000541913.5:c.-74+19000_-74+19009del (SPATA22) ENSP00000441920.1:n.-74+19000_-74+19009de...
ENST00000570318.1:c.-74+19199_-74+19208del (SPATA22) ENSP00000459147.1:n.-74+19199_-74+19208de...
NM_000049.2:c.689_698del (ASPA) NP_000040.1:p.Asp230GlyfsTer?
NM_001128085.1:c.689_698del (ASPA) NP_001121557.1:p.Asp230GlyfsTer?
XM_005256829.1:c.-74+19000_-74+19009del (SPATA22) XP_005256886.1:n.-74+19000_-74+19009del
XM_005256830.1:c.-74+19000_-74+19009del (SPATA22) XP_005256887.1:n.-74+19000_-74+19009del
XM_006721527.2:c.689_698del (ASPA) XP_006721590.1:p.Asp230GlyfsTer?
XR_934026.1:n.864_873del (ASPA)
NM_001321336.1:c.-74+19000_-74+19009del (SPATA22) NP_001308265.1:n.-74+19000_-74+19009del
NM_001321337.1:c.-74+19000_-74+19009del (SPATA22) NP_001308266.1:n.-74+19000_-74+19009del
XM_017024661.1:c.689_698del (ASPA) XP_016880150.1:p.Asp230GlyfsTer?
XM_024450764.1:c.689_698del (ASPA) XP_024306532.1:p.Asp230GlyfsTer?
XR_934026.2:n.864_873del (ASPA)
NM_000049.3:c.689_698del (ASPA) NP_000040.1:p.Asp230GlyfsTer?
NM_000049.4:c.689_698del (ASPA) MANE Select NP_000040.1:p.Asp230GlyfsTer?
NM_001321336.2:c.-74+19000_-74+19009del (SPATA22) NP_001308265.1:n.-74+19000_-74+19009del
NM_001321337.2:c.-74+19000_-74+19009del (SPATA22) NP_001308266.1:n.-74+19000_-74+19009del