Canonical Allele Identifier: CA672398217

Gene: SLC37A4

Linked Data

• dbSNP Id: rs1228313995
• MyVariant Identifiers: chr11:g.118901084G>T (hg19) ; chr11:g.119030374G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119030374G>T , CM000673.2:g.119030374G>T	GRCh38
NC_000011.9:g.118901084G>T , CM000673.1:g.118901084G>T	GRCh37
NC_000011.8:g.118406294G>T	NCBI36
NG_013331.1:g.5533C>A , LRG_187:g.5533C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.34+475C>A
ENST00000697846.1:n.34+475C>A
ENST00000697847.1:n.34+475C>A
ENST00000697848.1:n.34+475C>A
ENST00000697850.1:n.34+475C>A
ENST00000638360.1:n.42+475C>A
ENST00000638925.1:n.41+475C>A
ENST00000650539.1:n.6C>A
ENST00000330775.9:c.-196+475C>A	ENSP00000476242.2:n.-196+475C>A
ENST00000357590.9:c.-196+174C>A	ENSP00000476176.2:n.-196+174C>A
ENST00000525039.5:n.228+174C>A
ENST00000525102.5:n.420C>A
ENST00000527992.5:n.32+475C>A
ENST00000530407.5:n.24+475C>A
ENST00000532085.1:n.490C>A
ENST00000538950.5:c.-345+475C>A	ENSP00000475991.2:n.-345+475C>A
ENST00000545985.5:c.-338C>A	ENSP00000475241.2:n.-338C>A
NM_001164277.1:c.-338C>A , LRG_187t1:c.-338C>A	NP_001157749.1:n.-338C>A
NM_001164278.1:c.-196+174C>A	NP_001157750.1:n.-196+174C>A
NM_001164279.1:c.-345+475C>A	NP_001157751.1:n.-345+475C>A
NM_001467.5:c.-196+475C>A	NP_001458.1:n.-196+475C>A
NM_001164278.2:c.-196+174C>A	NP_001157750.1:n.-196+174C>A
NM_001164279.2:c.-345+475C>A	NP_001157751.1:n.-345+475C>A
NM_001467.6:c.-196+475C>A	NP_001458.1:n.-196+475C>A
NM_001164277.2:c.-338C>A MANE Select	NP_001157749.1:n.-338C>A