Canonical Allele Identifier: CA1829342392
Gene: SLC1A1 HGNC NCBI

Linked Data

dbSNP Id: rs1820837688

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.4507230_4507231del , CM000671.2:g.4507230_4507231del GRCh38
NC_000009.11:g.4507230_4507231del , CM000671.1:g.4507230_4507231del GRCh37
NC_000009.10:g.4497230_4497231del NCBI36
NG_017044.1:g.21804_21805del

Transcript Alleles

HGVS Amino-acid Change
ENST00000262352.8:c.91+16460_91+16461del MANE Select ENSP00000262352.3:n.91+16460_91+16461del
ENST00000262352.7:c.91+16460_91+16461del ENSP00000262352.3:n.91+16460_91+16461del
NM_004170.5:c.91+16460_91+16461del NP_004161.4:n.91+16460_91+16461del
XM_011518007.1:c.92-12598_92-12597del XP_011516309.1:n.92-12598_92-12597del
XM_011518010.1:c.91+16460_91+16461del XP_011516312.1:n.91+16460_91+16461del
XM_017015042.1:c.92-12598_92-12597del XP_016870531.1:n.92-12598_92-12597del
XM_017015043.1:c.91+16460_91+16461del XP_016870532.1:n.91+16460_91+16461del
NM_004170.6:c.91+16460_91+16461del MANE Select NP_004161.4:n.91+16460_91+16461del