Canonical Allele Identifier: CA13103826
Gene: SLC1A1 HGNC NCBI
SPATA6L HGNC NCBI

Linked Data

dbSNP Id: rs7856675
gnomAD v2: 9-4555305-A-G
gnomAD v3: 9-4555305-A-G
gnomAD v4: 9-4555305-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.4555305A>G , CM000671.2:g.4555305A>G GRCh38
NC_000009.11:g.4555305A>G , CM000671.1:g.4555305A>G GRCh37
NC_000009.10:g.4545305A>G NCBI36
NG_017044.1:g.69879A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000262352.8:c.233-6144A>G (SLC1A1) MANE Select ENSP00000262352.3:n.233-6144A>G
ENST00000262352.7:c.233-6144A>G (SLC1A1) ENSP00000262352.3:n.233-6144A>G
ENST00000485616.5:c.*782-917T>C (SPATA6L) ENSP00000420003.1:n.*782-917T>C
NM_004170.5:c.233-6144A>G (SLC1A1) NP_004161.4:n.233-6144A>G
XM_011518007.1:c.302-6144A>G (SLC1A1) XP_011516309.1:n.302-6144A>G
XM_011518008.1:c.242-6144A>G (SLC1A1) XP_011516310.1:n.242-6144A>G
XM_011518009.1:c.173-6144A>G (SLC1A1) XP_011516311.1:n.173-6144A>G
XM_011518010.1:c.92-6144A>G (SLC1A1) XP_011516312.1:n.92-6144A>G
XM_011518008.3:c.242-6144A>G (SLC1A1) XP_011516310.1:n.242-6144A>G
XM_011518009.3:c.173-6144A>G (SLC1A1) XP_011516311.1:n.173-6144A>G
XM_017014882.2:c.*2-14115T>C (SPATA6L) XP_016870371.1:n.*2-14115T>C
XM_017015042.1:c.302-6144A>G (SLC1A1) XP_016870531.1:n.302-6144A>G
XM_017015043.1:c.233-6144A>G (SLC1A1) XP_016870532.1:n.233-6144A>G
XR_001746335.2:n.1479-14115T>C (SPATA6L)
NM_004170.6:c.233-6144A>G (SLC1A1) MANE Select NP_004161.4:n.233-6144A>G