Canonical Allele Identifier: CA219288

Gene: SLC37A4

Linked Data

• ClinVar Variation Id: 68271
• ClinVar RCV Id: RCV000059121
• dbSNP Id: rs193302894
• MyVariant Identifiers: chr11:g.118899932C>G (hg19) ; chr11:g.119029222C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029222C>G , CM000673.2:g.119029222C>G	GRCh38
NC_000011.9:g.118899932C>G , CM000673.1:g.118899932C>G	GRCh37
NC_000011.8:g.118405142C>G	NCBI36
NG_013331.1:g.6685G>C , LRG_187:g.6685G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.377G>C
ENST00000697846.1:n.377G>C
ENST00000697847.1:n.377G>C
ENST00000697848.1:n.377G>C
ENST00000697849.1:n.621G>C
ENST00000697850.1:n.377G>C
ENST00000697851.1:n.621G>C
ENST00000638186.1:n.451G>C
ENST00000638360.1:n.385G>C
ENST00000638925.1:n.384G>C
ENST00000650539.1:n.553G>C
ENST00000330775.9:c.148G>C	ENSP00000476242.2:p.Gly50Arg
ENST00000357590.9:c.148G>C	ENSP00000476176.2:p.Gly50Arg
ENST00000524428.5:n.148G>C
ENST00000525039.5:n.571G>C
ENST00000525102.5:n.905G>C
ENST00000525372.5:n.148G>C
ENST00000525787.1:n.443G>C
ENST00000526626.6:n.343G>C
ENST00000527992.5:n.375G>C
ENST00000529510.5:n.166G>C
ENST00000530407.5:n.197+170G>C
ENST00000532085.1:n.1642G>C
ENST00000532888.6:n.343G>C
ENST00000534384.1:n.368G>C
ENST00000538950.5:c.-172+170G>C	ENSP00000475991.2:n.-172+170G>C
ENST00000545985.5:c.148G>C	ENSP00000475241.2:p.Gly50Arg
NM_001164277.1:c.148G>C , LRG_187t1:c.148G>C	NP_001157749.1:p.Gly50Arg
NM_001164278.1:c.148G>C	NP_001157750.1:p.Gly50Arg
NM_001164279.1:c.-172+170G>C	NP_001157751.1:n.-172+170G>C
NM_001164280.1:c.148G>C	NP_001157752.1:p.Gly50Arg
NM_001467.5:c.148G>C	NP_001458.1:p.Gly50Arg
NM_001164278.2:c.148G>C	NP_001157750.1:p.Gly50Arg
NM_001164279.2:c.-172+170G>C	NP_001157751.1:n.-172+170G>C
NM_001164280.2:c.148G>C	NP_001157752.1:p.Gly50Arg
NM_001467.6:c.148G>C	NP_001458.1:p.Gly50Arg
NM_001164277.2:c.148G>C MANE Select	NP_001157749.1:p.Gly50Arg