Canonical Allele Identifier: CA188364644

Gene: SLC1A1

Linked Data

• dbSNP Id: rs576352787
• gnomAD v2: 9-4507446-T-C
• gnomAD v3: 9-4507446-T-C
• gnomAD v4: 9-4507446-T-C
• MyVariant Identifiers: chr9:g.4507446T>C (hg19) ; chr9:g.4507446T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.4507446T>C , CM000671.2:g.4507446T>C	GRCh38
NC_000009.11:g.4507446T>C , CM000671.1:g.4507446T>C	GRCh37
NC_000009.10:g.4497446T>C	NCBI36
NG_017044.1:g.22020T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000262352.8:c.91+16676T>C MANE Select	ENSP00000262352.3:n.91+16676T>C
ENST00000262352.7:c.91+16676T>C	ENSP00000262352.3:n.91+16676T>C
NM_004170.5:c.91+16676T>C	NP_004161.4:n.91+16676T>C
XM_011518007.1:c.92-12382T>C	XP_011516309.1:n.92-12382T>C
XM_011518010.1:c.91+16676T>C	XP_011516312.1:n.91+16676T>C
XM_017015042.1:c.92-12382T>C	XP_016870531.1:n.92-12382T>C
XM_017015043.1:c.91+16676T>C	XP_016870532.1:n.91+16676T>C
NM_004170.6:c.91+16676T>C MANE Select	NP_004161.4:n.91+16676T>C