Canonical Allele Identifier: CA728316468
Gene: ASPA HGNC NCBI
SPATA22 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.3498792A>T , CM000679.2:g.3498792A>T GRCh38
NC_000017.10:g.3402086A>T , CM000679.1:g.3402086A>T GRCh37
NC_000017.9:g.3348836A>T NCBI36
NG_008399.1:g.29683A>T
NG_008399.2:g.30147A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000263080.3:c.745-99A>T (ASPA) MANE Select ENSP00000263080.2:p.=
ENST00000263080.2:c.745-99A>T ENSP00000263080.2:p.=
ENST00000456349.6:c.745-99A>T ENSP00000409976.2:p.=
ENST00000541913.5:c.-74+14620T>A ENSP00000441920.1:p.=
ENST00000570318.1:c.-74+14819T>A ENSP00000459147.1:p.=
NM_000049.2:c.745-99A>T (ASPA) NP_000040.1:p.=
NM_001128085.1:c.745-99A>T (ASPA) NP_001121557.1:p.=
XM_005256829.1:c.-74+14620T>A (SPATA22) XP_005256886.1:p.=
XM_005256830.1:c.-74+14620T>A (SPATA22) XP_005256887.1:p.=
XM_006721527.2:c.745-99A>T (ASPA) XP_006721590.1:p.=
XR_934026.1:n.1012-99A>T (ASPA)
NM_001321336.1:c.-74+14620T>A (SPATA22) NP_001308265.1:p.=
NM_001321337.1:c.-74+14620T>A (SPATA22) NP_001308266.1:p.=
XM_017024661.1:c.745-99A>T (ASPA) XP_016880150.1:p.=
XM_024450764.1:c.745-99A>T (ASPA) XP_024306532.1:p.=
XR_934026.2:n.1012-99A>T (ASPA)
NM_000049.3:c.745-99A>T (ASPA) NP_000040.1:p.=
NM_000049.4:c.745-99A>T (ASPA) MANE Select NP_000040.1:p.=
NM_001321336.2:c.-74+14620T>A (SPATA22) NP_001308265.1:p.=
NM_001321337.2:c.-74+14620T>A (SPATA22) NP_001308266.1:p.=