Canonical Allele Identifier: CA2243897680
Gene: ASPA HGNC NCBI
SPATA22 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.3499452_3499459delinsCTTGTACT , CM000679.2:g.3499452_3499459delinsCTTGTACT GRCh38
NC_000017.10:g.3402746_3402753delinsCTTGTACT , CM000679.1:g.3402746_3402753delinsCTTGTACT GRCh37
NC_000017.9:g.3349496_3349503delinsCTTGTACT NCBI36
NG_008399.1:g.30343_30350delinsCTTGTACT
NG_008399.2:g.30807_30814delinsCTTGTACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000263080.3:c.*364_*371delinsCTTGTACT (ASPA) MANE Select ENSP00000263080.2:n.*364_*371delinsCTTGTACT
ENST00000263080.2:c.*364_*371delinsCTTGTACT (ASPA) ENSP00000263080.2:n.*364_*371delinsCTTGTACT
ENST00000541913.5:c.-74+13953_-74+13960delinsAGTACAAG (SPATA22) ENSP00000441920.1:n.-74+13953_-74+13960delinsAGTACAAG
ENST00000570318.1:c.-74+14152_-74+14159delinsAGTACAAG (SPATA22) ENSP00000459147.1:n.-74+14152_-74+14159delinsAGTACAAG
XM_005256829.1:c.-74+13953_-74+13960delinsAGTACAAG (SPATA22) XP_005256886.1:n.-74+13953_-74+13960delinsAGTACAAG
XM_005256830.1:c.-74+13953_-74+13960delinsAGTACAAG (SPATA22) XP_005256887.1:n.-74+13953_-74+13960delinsAGTACAAG
NM_001321336.1:c.-74+13953_-74+13960delinsAGTACAAG (SPATA22) NP_001308265.1:n.-74+13953_-74+13960delinsAGTACAAG
NM_001321337.1:c.-74+13953_-74+13960delinsAGTACAAG (SPATA22) NP_001308266.1:n.-74+13953_-74+13960delinsAGTACAAG
XM_017024661.1:c.*364_*371delinsCTTGTACT (ASPA) XP_016880150.1:n.*364_*371delinsCTTGTACT
XM_024450764.1:c.*364_*371delinsCTTGTACT (ASPA) XP_024306532.1:n.*364_*371delinsCTTGTACT
NM_000049.3:c.*364_*371delinsCTTGTACT (ASPA) NP_000040.1:n.*364_*371delinsCTTGTACT
NM_000049.4:c.*364_*371delinsCTTGTACT (ASPA) MANE Select NP_000040.1:n.*364_*371delinsCTTGTACT
NM_001321336.2:c.-74+13953_-74+13960delinsAGTACAAG (SPATA22) NP_001308265.1:n.-74+13953_-74+13960delinsAGTACAAG
NM_001321337.2:c.-74+13953_-74+13960delinsAGTACAAG (SPATA22) NP_001308266.1:n.-74+13953_-74+13960delinsAGTACAAG