Canonical Allele Identifier: CA1829385757

Gene: SLC1A1 SPATA6L

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.4576799T= , CM000671.2:g.4576799T=	GRCh38
NC_000009.11:g.4576799T= , CM000671.1:g.4576799T=	GRCh37
NC_000009.10:g.4566799T=	NCBI36
NG_017044.1:g.91373T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000262352.8:c.1193+36T= (SLC1A1) MANE Select	ENSP00000262352.3:n.1193+36T=
ENST00000262352.7:c.1193+36T= (SLC1A1)	ENSP00000262352.3:n.1193+36T=
ENST00000422398.1:c.480+36T= (SLC1A1)
ENST00000485616.5:c.*782-22411A= (SPATA6L)	ENSP00000420003.1:n.*782-22411A=
NM_004170.5:c.1193+36T= (SLC1A1)	NP_004161.4:n.1193+36T=
XM_011518007.1:c.1262+36T= (SLC1A1)	XP_011516309.1:n.1262+36T=
XM_011518008.1:c.1202+36T= (SLC1A1)	XP_011516310.1:n.1202+36T=
XM_011518009.1:c.1133+36T= (SLC1A1)	XP_011516311.1:n.1133+36T=
XM_011518010.1:c.1052+36T= (SLC1A1)	XP_011516312.1:n.1052+36T=
XM_011518008.3:c.1202+36T= (SLC1A1)	XP_011516310.1:n.1202+36T=
XM_011518009.3:c.1133+36T= (SLC1A1)	XP_011516311.1:n.1133+36T=
XM_017014882.2:c.*1+27380A= (SPATA6L)	XP_016870371.1:n.*1+27380A=
XM_017015042.1:c.1154+36T= (SLC1A1)	XP_016870531.1:n.1154+36T=
XM_017015043.1:c.1085+36T= (SLC1A1)	XP_016870532.1:n.1085+36T=
XR_001746335.2:n.1478+23854A= (SPATA6L)
NM_004170.6:c.1193+36T= (SLC1A1) MANE Select	NP_004161.4:n.1193+36T=