Canonical Allele Identifier: CA2243882283
Gene: ASPA HGNC NCBI
SPATA22 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.3481377G= , CM000679.2:g.3481377G= GRCh38
NC_000017.10:g.3384671G= , CM000679.1:g.3384671G= GRCh37
NC_000017.9:g.3331421G= NCBI36
NG_008399.1:g.12268G=
NG_008399.2:g.12732G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263080.3:c.237-226G= (ASPA) MANE Select ENSP00000263080.2:n.237-226G=
ENST00000263080.2:c.237-226G= (ASPA) ENSP00000263080.2:n.237-226G=
ENST00000456349.6:c.237-226G= (ASPA) ENSP00000409976.2:n.237-226G=
ENST00000541913.5:c.-73-11979C= (SPATA22) ENSP00000441920.1:n.-73-11979C=
ENST00000570318.1:c.-73-11979C= (SPATA22) ENSP00000459147.1:n.-73-11979C=
ENST00000571278.1:c.142-226G= (ASPA) ENSP00000461358.1:n.142-226G=
NM_000049.2:c.237-226G= (ASPA) NP_000040.1:n.237-226G=
NM_001128085.1:c.237-226G= (ASPA) NP_001121557.1:n.237-226G=
XM_005256829.1:c.-73-11979C= (SPATA22) XP_005256886.1:n.-73-11979C=
XM_005256830.1:c.-73-11979C= (SPATA22) XP_005256887.1:n.-73-11979C=
XM_006721527.2:c.237-226G= (ASPA) XP_006721590.1:n.237-226G=
XR_934026.1:n.412-226G= (ASPA)
NM_001321336.1:c.-73-11979C= (SPATA22) NP_001308265.1:n.-73-11979C=
NM_001321337.1:c.-73-11979C= (SPATA22) NP_001308266.1:n.-73-11979C=
XM_017024661.1:c.237-226G= (ASPA) XP_016880150.1:n.237-226G=
XM_024450764.1:c.237-226G= (ASPA) XP_024306532.1:n.237-226G=
XR_934026.2:n.412-226G= (ASPA)
NM_000049.3:c.237-226G= (ASPA) NP_000040.1:n.237-226G=
NM_000049.4:c.237-226G= (ASPA) MANE Select NP_000040.1:n.237-226G=
NM_001321336.2:c.-73-11979C= (SPATA22) NP_001308265.1:n.-73-11979C=
NM_001321337.2:c.-73-11979C= (SPATA22) NP_001308266.1:n.-73-11979C=