Canonical Allele Identifier: CA397687729

Gene: ASPA SPATA22

Linked Data

• ClinVar Variation Id: 2907869
• ClinVar RCV Id: RCV003606892
• MyVariant Identifiers: chr17:g.3402300C>T (hg19) ; chr17:g.3499006C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.3499006C>T , CM000679.2:g.3499006C>T	GRCh38
NC_000017.10:g.3402300C>T , CM000679.1:g.3402300C>T	GRCh37
NC_000017.9:g.3349050C>T	NCBI36
NG_008399.1:g.29897C>T
NG_008399.2:g.30361C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000263080.3:c.860C>T (ASPA) MANE Select	ENSP00000263080.2:p.Ala287Val
ENST00000263080.2:c.860C>T (ASPA)	ENSP00000263080.2:p.Ala287Val
ENST00000456349.6:c.860C>T (ASPA)	ENSP00000409976.2:p.Ala287Val
ENST00000541913.5:c.-74+14406G>A (SPATA22)	ENSP00000441920.1:n.-74+14406G>A
ENST00000570318.1:c.-74+14605G>A (SPATA22)	ENSP00000459147.1:n.-74+14605G>A
NM_000049.2:c.860C>T (ASPA)	NP_000040.1:p.Ala287Val
NM_001128085.1:c.860C>T (ASPA)	NP_001121557.1:p.Ala287Val
XM_005256829.1:c.-74+14406G>A (SPATA22)	XP_005256886.1:n.-74+14406G>A
XM_005256830.1:c.-74+14406G>A (SPATA22)	XP_005256887.1:n.-74+14406G>A
XM_006721527.2:c.860C>T (ASPA)	XP_006721590.1:p.Ala287Val
NM_001321336.1:c.-74+14406G>A (SPATA22)	NP_001308265.1:n.-74+14406G>A
NM_001321337.1:c.-74+14406G>A (SPATA22)	NP_001308266.1:n.-74+14406G>A
XM_017024661.1:c.860C>T (ASPA)	XP_016880150.1:p.Ala287Val
XM_024450764.1:c.860C>T (ASPA)	XP_024306532.1:p.Ala287Val
XR_934026.2:n.1127C>T (ASPA)
NM_000049.3:c.860C>T (ASPA)	NP_000040.1:p.Ala287Val
NM_000049.4:c.860C>T (ASPA) MANE Select	NP_000040.1:p.Ala287Val
NM_001321336.2:c.-74+14406G>A (SPATA22)	NP_001308265.1:n.-74+14406G>A
NM_001321337.2:c.-74+14406G>A (SPATA22)	NP_001308266.1:n.-74+14406G>A