Canonical Allele Identifier: CA2689285221

Gene: SLC1A1 SPATA6L

Linked Data

• gnomAD v4: 9-4576800-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.4576800_4576801insT , CM000671.2:g.4576800_4576801insT	GRCh38
NC_000009.11:g.4576800_4576801insT , CM000671.1:g.4576800_4576801insT	GRCh37
NC_000009.10:g.4566800_4566801insT	NCBI36
NG_017044.1:g.91374_91375insT

Transcript Alleles

HGVS	Amino-acid change
ENST00000262352.8:c.1193+37_1193+38insT (SLC1A1) MANE Select	ENSP00000262352.3:n.1193+37_1193+38insT
ENST00000262352.7:c.1193+37_1193+38insT (SLC1A1)	ENSP00000262352.3:n.1193+37_1193+38insT
ENST00000422398.1:c.480+37_480+38insT (SLC1A1)
ENST00000485616.5:c.*782-22413_*782-22412insA (SPATA6L)	ENSP00000420003.1:n.*782-22413_*782-22412...
NM_004170.5:c.1193+37_1193+38insT (SLC1A1)	NP_004161.4:n.1193+37_1193+38insT
XM_011518007.1:c.1262+37_1262+38insT (SLC1A1)	XP_011516309.1:n.1262+37_1262+38insT
XM_011518008.1:c.1202+37_1202+38insT (SLC1A1)	XP_011516310.1:n.1202+37_1202+38insT
XM_011518009.1:c.1133+37_1133+38insT (SLC1A1)	XP_011516311.1:n.1133+37_1133+38insT
XM_011518010.1:c.1052+37_1052+38insT (SLC1A1)	XP_011516312.1:n.1052+37_1052+38insT
XM_011518008.3:c.1202+37_1202+38insT (SLC1A1)	XP_011516310.1:n.1202+37_1202+38insT
XM_011518009.3:c.1133+37_1133+38insT (SLC1A1)	XP_011516311.1:n.1133+37_1133+38insT
XM_017014882.2:c.*1+27378_*1+27379insA (SPATA6L)	XP_016870371.1:n.*1+27378_*1+27379insA
XM_017015042.1:c.1154+37_1154+38insT (SLC1A1)	XP_016870531.1:n.1154+37_1154+38insT
XM_017015043.1:c.1085+37_1085+38insT (SLC1A1)	XP_016870532.1:n.1085+37_1085+38insT
XR_001746335.2:n.1478+23852_1478+23853insA (SPATA6L)
NM_004170.6:c.1193+37_1193+38insT (SLC1A1) MANE Select	NP_004161.4:n.1193+37_1193+38insT