Canonical Allele Identifier: CA1829342501
Gene: SLC1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.4507465_4507474delinsCTTAAATTCT , CM000671.2:g.4507465_4507474delinsCTTAAATTCT GRCh38
NC_000009.11:g.4507465_4507474delinsCTTAAATTCT , CM000671.1:g.4507465_4507474delinsCTTAAATTCT GRCh37
NC_000009.10:g.4497465_4497474delinsCTTAAATTCT NCBI36
NG_017044.1:g.22039_22048delinsCTTAAATTCT

Transcript Alleles

HGVS Amino-acid change
ENST00000262352.8:c.91+16695_91+16704delinsCTTAAATTCT MANE Select ENSP00000262352.3:n.91+16695_91+16704deli...
ENST00000262352.7:c.91+16695_91+16704delinsCTTAAATTCT ENSP00000262352.3:n.91+16695_91+16704deli...
NM_004170.5:c.91+16695_91+16704delinsCTTAAATTCT NP_004161.4:n.91+16695_91+16704delinsCTTA...
XM_011518007.1:c.92-12363_92-12354delinsCTTAAATTCT XP_011516309.1:n.92-12363_92-12354delinsC...
XM_011518010.1:c.91+16695_91+16704delinsCTTAAATTCT XP_011516312.1:n.91+16695_91+16704delinsC...
XM_017015042.1:c.92-12363_92-12354delinsCTTAAATTCT XP_016870531.1:n.92-12363_92-12354delinsC...
XM_017015043.1:c.91+16695_91+16704delinsCTTAAATTCT XP_016870532.1:n.91+16695_91+16704delinsC...
NM_004170.6:c.91+16695_91+16704delinsCTTAAATTCT MANE Select NP_004161.4:n.91+16695_91+16704delinsCTTA...