Canonical Allele Identifier: CA2243897706

Gene: ASPA SPATA22

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.3499458_3499459delinsCT , CM000679.2:g.3499458_3499459delinsCT	GRCh38
NC_000017.10:g.3402752_3402753delinsCT , CM000679.1:g.3402752_3402753delinsCT	GRCh37
NC_000017.9:g.3349502_3349503delinsCT	NCBI36
NG_008399.1:g.30349_30350delinsCT
NG_008399.2:g.30813_30814delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263080.3:c.*370_*371delinsCT (ASPA) MANE Select	ENSP00000263080.2:n.*370_*371delinsCT
ENST00000263080.2:c.*370_*371delinsCT (ASPA)	ENSP00000263080.2:n.*370_*371delinsCT
ENST00000541913.5:c.-74+13953_-74+13954delinsAG (SPATA22)	ENSP00000441920.1:n.-74+13953_-74+13954delinsAG
ENST00000570318.1:c.-74+14152_-74+14153delinsAG (SPATA22)	ENSP00000459147.1:n.-74+14152_-74+14153delinsAG
XM_005256829.1:c.-74+13953_-74+13954delinsAG (SPATA22)	XP_005256886.1:n.-74+13953_-74+13954delinsAG
XM_005256830.1:c.-74+13953_-74+13954delinsAG (SPATA22)	XP_005256887.1:n.-74+13953_-74+13954delinsAG
NM_001321336.1:c.-74+13953_-74+13954delinsAG (SPATA22)	NP_001308265.1:n.-74+13953_-74+13954delinsAG
NM_001321337.1:c.-74+13953_-74+13954delinsAG (SPATA22)	NP_001308266.1:n.-74+13953_-74+13954delinsAG
XM_017024661.1:c.*370_*371delinsCT (ASPA)	XP_016880150.1:n.*370_*371delinsCT
XM_024450764.1:c.*370_*371delinsCT (ASPA)	XP_024306532.1:n.*370_*371delinsCT
NM_000049.3:c.*370_*371delinsCT (ASPA)	NP_000040.1:n.*370_*371delinsCT
NM_000049.4:c.*370_*371delinsCT (ASPA) MANE Select	NP_000040.1:n.*370_*371delinsCT
NM_001321336.2:c.-74+13953_-74+13954delinsAG (SPATA22)	NP_001308265.1:n.-74+13953_-74+13954delinsAG
NM_001321337.2:c.-74+13953_-74+13954delinsAG (SPATA22)	NP_001308266.1:n.-74+13953_-74+13954delinsAG