Canonical Allele Identifier: CA372818566
Gene: SLC1A1 HGNC NCBI
SPATA6L HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.4576684C>T , CM000671.2:g.4576684C>T GRCh38
NC_000009.11:g.4576684C>T , CM000671.1:g.4576684C>T GRCh37
NC_000009.10:g.4566684C>T NCBI36
NG_017044.1:g.91258C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000262352.8:c.1114C>T (SLC1A1) MANE Select ENSP00000262352.3:p.Leu372Phe
ENST00000262352.7:c.1114C>T (SLC1A1) ENSP00000262352.3:p.Leu372Phe
ENST00000422398.1:c.401C>T (SLC1A1)
ENST00000485616.5:c.*782-22296G>A (SPATA6L) ENSP00000420003.1:n.*782-22296G>A
NM_004170.5:c.1114C>T (SLC1A1) NP_004161.4:p.Leu372Phe
XM_011518007.1:c.1183C>T (SLC1A1) XP_011516309.1:p.Leu395Phe
XM_011518008.1:c.1123C>T (SLC1A1) XP_011516310.1:p.Leu375Phe
XM_011518009.1:c.1054C>T (SLC1A1) XP_011516311.1:p.Leu352Phe
XM_011518010.1:c.973C>T (SLC1A1) XP_011516312.1:p.Leu325Phe
XM_011518008.3:c.1123C>T (SLC1A1) XP_011516310.1:p.Leu375Phe
XM_011518009.3:c.1054C>T (SLC1A1) XP_011516311.1:p.Leu352Phe
XM_017014882.2:c.*1+27495G>A (SPATA6L) XP_016870371.1:n.*1+27495G>A
XM_017015042.1:c.1075C>T (SLC1A1) XP_016870531.1:p.Leu359Phe
XM_017015043.1:c.1006C>T (SLC1A1) XP_016870532.1:p.Leu336Phe
XR_001746335.2:n.1478+23969G>A (SPATA6L)
NM_004170.6:c.1114C>T (SLC1A1) MANE Select NP_004161.4:p.Leu372Phe