Canonical Allele Identifier: CA4968996
Gene: SLC1A1 HGNC NCBI
SPATA6L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.4566036G>A , CM000671.2:g.4566036G>A GRCh38
NC_000009.11:g.4566036G>A , CM000671.1:g.4566036G>A GRCh37
NC_000009.10:g.4556036G>A NCBI36
NG_017044.1:g.80610G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262352.8:c.441-11G>A (SLC1A1) MANE Select ENSP00000262352.3:n.441-11G>A
ENST00000262352.7:c.441-11G>A (SLC1A1) ENSP00000262352.3:n.441-11G>A
ENST00000485616.5:c.*782-11648C>T (SPATA6L) ENSP00000420003.1:n.*782-11648C>T
NM_004170.5:c.441-11G>A (SLC1A1) NP_004161.4:n.441-11G>A
XM_011518007.1:c.510-11G>A (SLC1A1) XP_011516309.1:n.510-11G>A
XM_011518008.1:c.450-11G>A (SLC1A1) XP_011516310.1:n.450-11G>A
XM_011518009.1:c.381-11G>A (SLC1A1) XP_011516311.1:n.381-11G>A
XM_011518010.1:c.300-11G>A (SLC1A1) XP_011516312.1:n.300-11G>A
XM_011518008.3:c.450-11G>A (SLC1A1) XP_011516310.1:n.450-11G>A
XM_011518009.3:c.381-11G>A (SLC1A1) XP_011516311.1:n.381-11G>A
XM_017014882.2:c.*2-24846C>T (SPATA6L) XP_016870371.1:n.*2-24846C>T
XM_017015042.1:c.510-11G>A (SLC1A1) XP_016870531.1:n.510-11G>A
XM_017015043.1:c.441-11G>A (SLC1A1) XP_016870532.1:n.441-11G>A
XR_001746335.2:n.1479-24846C>T (SPATA6L)
NM_004170.6:c.441-11G>A (SLC1A1) MANE Select NP_004161.4:n.441-11G>A