Canonical Allele Identifier: CA4969258
Gene: SLC1A1 HGNC NCBI
SPATA6L HGNC NCBI

Linked Data

dbSNP Id: rs770847366
gnomAD v2: 9-4576799-T-A
gnomAD v4: 9-4576799-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.4576799T>A , CM000671.2:g.4576799T>A GRCh38
NC_000009.11:g.4576799T>A , CM000671.1:g.4576799T>A GRCh37
NC_000009.10:g.4566799T>A NCBI36
NG_017044.1:g.91373T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000262352.8:c.1193+36T>A (SLC1A1) MANE Select ENSP00000262352.3:n.1193+36T>A
ENST00000262352.7:c.1193+36T>A (SLC1A1) ENSP00000262352.3:n.1193+36T>A
ENST00000422398.1:c.480+36T>A (SLC1A1)
ENST00000485616.5:c.*782-22411A>T (SPATA6L) ENSP00000420003.1:n.*782-22411A>T
NM_004170.5:c.1193+36T>A (SLC1A1) NP_004161.4:n.1193+36T>A
XM_011518007.1:c.1262+36T>A (SLC1A1) XP_011516309.1:n.1262+36T>A
XM_011518008.1:c.1202+36T>A (SLC1A1) XP_011516310.1:n.1202+36T>A
XM_011518009.1:c.1133+36T>A (SLC1A1) XP_011516311.1:n.1133+36T>A
XM_011518010.1:c.1052+36T>A (SLC1A1) XP_011516312.1:n.1052+36T>A
XM_011518008.3:c.1202+36T>A (SLC1A1) XP_011516310.1:n.1202+36T>A
XM_011518009.3:c.1133+36T>A (SLC1A1) XP_011516311.1:n.1133+36T>A
XM_017014882.2:c.*1+27380A>T (SPATA6L) XP_016870371.1:n.*1+27380A>T
XM_017015042.1:c.1154+36T>A (SLC1A1) XP_016870531.1:n.1154+36T>A
XM_017015043.1:c.1085+36T>A (SLC1A1) XP_016870532.1:n.1085+36T>A
XR_001746335.2:n.1478+23854A>T (SPATA6L)
NM_004170.6:c.1193+36T>A (SLC1A1) MANE Select NP_004161.4:n.1193+36T>A