Canonical Allele Identifier: CA2243896796
Gene: ASPA HGNC NCBI
SPATA22 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.3498843A= , CM000679.2:g.3498843A= GRCh38
NC_000017.10:g.3402137A= , CM000679.1:g.3402137A= GRCh37
NC_000017.9:g.3348887A= NCBI36
NG_008399.1:g.29734A=
NG_008399.2:g.30198A=

Transcript Alleles

HGVS Amino-acid change
ENST00000263080.3:c.745-48A= (ASPA) MANE Select ENSP00000263080.2:n.745-48A=
ENST00000263080.2:c.745-48A= (ASPA) ENSP00000263080.2:n.745-48A=
ENST00000456349.6:c.745-48A= (ASPA) ENSP00000409976.2:n.745-48A=
ENST00000541913.5:c.-74+14569T= (SPATA22) ENSP00000441920.1:n.-74+14569T=
ENST00000570318.1:c.-74+14768T= (SPATA22) ENSP00000459147.1:n.-74+14768T=
NM_000049.2:c.745-48A= (ASPA) NP_000040.1:n.745-48A=
NM_001128085.1:c.745-48A= (ASPA) NP_001121557.1:n.745-48A=
XM_005256829.1:c.-74+14569T= (SPATA22) XP_005256886.1:n.-74+14569T=
XM_005256830.1:c.-74+14569T= (SPATA22) XP_005256887.1:n.-74+14569T=
XM_006721527.2:c.745-48A= (ASPA) XP_006721590.1:n.745-48A=
XR_934026.1:n.1012-48A= (ASPA)
NM_001321336.1:c.-74+14569T= (SPATA22) NP_001308265.1:n.-74+14569T=
NM_001321337.1:c.-74+14569T= (SPATA22) NP_001308266.1:n.-74+14569T=
XM_017024661.1:c.745-48A= (ASPA) XP_016880150.1:n.745-48A=
XM_024450764.1:c.745-48A= (ASPA) XP_024306532.1:n.745-48A=
XR_934026.2:n.1012-48A= (ASPA)
NM_000049.3:c.745-48A= (ASPA) NP_000040.1:n.745-48A=
NM_000049.4:c.745-48A= (ASPA) MANE Select NP_000040.1:n.745-48A=
NM_001321336.2:c.-74+14569T= (SPATA22) NP_001308265.1:n.-74+14569T=
NM_001321337.2:c.-74+14569T= (SPATA22) NP_001308266.1:n.-74+14569T=