Canonical Allele Identifier: CA2243897678

Gene: ASPA SPATA22

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.3499451_3499456delinsACTTGT , CM000679.2:g.3499451_3499456delinsACTTGT	GRCh38
NC_000017.10:g.3402745_3402750delinsACTTGT , CM000679.1:g.3402745_3402750delinsACTTGT	GRCh37
NC_000017.9:g.3349495_3349500delinsACTTGT	NCBI36
NG_008399.1:g.30342_30347delinsACTTGT
NG_008399.2:g.30806_30811delinsACTTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263080.3:c.*363_*368delinsACTTGT (ASPA) MANE Select	ENSP00000263080.2:n.*363_*368delinsACTTGT
ENST00000263080.2:c.*363_*368delinsACTTGT (ASPA)	ENSP00000263080.2:n.*363_*368delinsACTTGT
ENST00000541913.5:c.-74+13956_-74+13961delinsACAAGT (SPATA22)	ENSP00000441920.1:n.-74+13956_-74+13961delinsACAAGT
ENST00000570318.1:c.-74+14155_-74+14160delinsACAAGT (SPATA22)	ENSP00000459147.1:n.-74+14155_-74+14160delinsACAAGT
XM_005256829.1:c.-74+13956_-74+13961delinsACAAGT (SPATA22)	XP_005256886.1:n.-74+13956_-74+13961delinsACAAGT
XM_005256830.1:c.-74+13956_-74+13961delinsACAAGT (SPATA22)	XP_005256887.1:n.-74+13956_-74+13961delinsACAAGT
NM_001321336.1:c.-74+13956_-74+13961delinsACAAGT (SPATA22)	NP_001308265.1:n.-74+13956_-74+13961delinsACAAGT
NM_001321337.1:c.-74+13956_-74+13961delinsACAAGT (SPATA22)	NP_001308266.1:n.-74+13956_-74+13961delinsACAAGT
XM_017024661.1:c.*363_*368delinsACTTGT (ASPA)	XP_016880150.1:n.*363_*368delinsACTTGT
XM_024450764.1:c.*363_*368delinsACTTGT (ASPA)	XP_024306532.1:n.*363_*368delinsACTTGT
NM_000049.3:c.*363_*368delinsACTTGT (ASPA)	NP_000040.1:n.*363_*368delinsACTTGT
NM_000049.4:c.*363_*368delinsACTTGT (ASPA) MANE Select	NP_000040.1:n.*363_*368delinsACTTGT
NM_001321336.2:c.-74+13956_-74+13961delinsACAAGT (SPATA22)	NP_001308265.1:n.-74+13956_-74+13961delinsACAAGT
NM_001321337.2:c.-74+13956_-74+13961delinsACAAGT (SPATA22)	NP_001308266.1:n.-74+13956_-74+13961delinsACAAGT