Canonical Allele Identifier: CA2689285219
Gene: SLC1A1 HGNC NCBI
SPATA6L HGNC NCBI

Linked Data

gnomAD v4: 9-4576797-GA-G

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.4576798del , CM000671.2:g.4576798del GRCh38
NC_000009.11:g.4576798del , CM000671.1:g.4576798del GRCh37
NC_000009.10:g.4566798del NCBI36
NG_017044.1:g.91372del

Transcript Alleles

HGVS Amino-acid change
ENST00000262352.8:c.1193+35del (SLC1A1) MANE Select ENSP00000262352.3:n.1193+35del
ENST00000262352.7:c.1193+35del (SLC1A1) ENSP00000262352.3:n.1193+35del
ENST00000422398.1:c.480+35del (SLC1A1)
ENST00000485616.5:c.*782-22410del (SPATA6L) ENSP00000420003.1:n.*782-22410del
NM_004170.5:c.1193+35del (SLC1A1) NP_004161.4:n.1193+35del
XM_011518007.1:c.1262+35del (SLC1A1) XP_011516309.1:n.1262+35del
XM_011518008.1:c.1202+35del (SLC1A1) XP_011516310.1:n.1202+35del
XM_011518009.1:c.1133+35del (SLC1A1) XP_011516311.1:n.1133+35del
XM_011518010.1:c.1052+35del (SLC1A1) XP_011516312.1:n.1052+35del
XM_011518008.3:c.1202+35del (SLC1A1) XP_011516310.1:n.1202+35del
XM_011518009.3:c.1133+35del (SLC1A1) XP_011516311.1:n.1133+35del
XM_017014882.2:c.*1+27381del (SPATA6L) XP_016870371.1:n.*1+27381del
XM_017015042.1:c.1154+35del (SLC1A1) XP_016870531.1:n.1154+35del
XM_017015043.1:c.1085+35del (SLC1A1) XP_016870532.1:n.1085+35del
XR_001746335.2:n.1478+23855del (SPATA6L)
NM_004170.6:c.1193+35del (SLC1A1) MANE Select NP_004161.4:n.1193+35del