Canonical Allele Identifier: CA382908416

Gene: SLC37A4

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029276A>G , CM000673.2:g.119029276A>G	GRCh38
NC_000011.9:g.118899986A>G , CM000673.1:g.118899986A>G	GRCh37
NC_000011.8:g.118405196A>G	NCBI36
NG_013331.1:g.6631T>C , LRG_187:g.6631T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.323T>C
ENST00000697846.1:n.323T>C
ENST00000697847.1:n.323T>C
ENST00000697848.1:n.323T>C
ENST00000697849.1:n.567T>C
ENST00000697850.1:n.323T>C
ENST00000697851.1:n.567T>C
ENST00000638186.1:n.397T>C
ENST00000638360.1:n.331T>C
ENST00000638925.1:n.330T>C
ENST00000650539.1:n.499T>C
ENST00000330775.9:c.94T>C	ENSP00000476242.2:p.Ser32Pro
ENST00000357590.9:c.94T>C	ENSP00000476176.2:p.Ser32Pro
ENST00000524428.5:n.94T>C
ENST00000525039.5:n.517T>C
ENST00000525102.5:n.851T>C
ENST00000525372.5:n.94T>C
ENST00000525787.1:n.389T>C
ENST00000526626.6:n.289T>C
ENST00000527992.5:n.321T>C
ENST00000529510.5:n.112T>C
ENST00000530407.5:n.197+116T>C
ENST00000532085.1:n.1588T>C
ENST00000532888.6:n.289T>C
ENST00000534384.1:n.314T>C
ENST00000538950.5:c.-172+116T>C	ENSP00000475991.2:n.-172+116T>C
ENST00000545985.5:c.94T>C	ENSP00000475241.2:p.Ser32Pro
NM_001164277.1:c.94T>C , LRG_187t1:c.94T>C	NP_001157749.1:p.Ser32Pro
NM_001164278.1:c.94T>C	NP_001157750.1:p.Ser32Pro
NM_001164279.1:c.-172+116T>C	NP_001157751.1:n.-172+116T>C
NM_001164280.1:c.94T>C	NP_001157752.1:p.Ser32Pro
NM_001467.5:c.94T>C	NP_001458.1:p.Ser32Pro
NM_001164278.2:c.94T>C	NP_001157750.1:p.Ser32Pro
NM_001164279.2:c.-172+116T>C	NP_001157751.1:n.-172+116T>C
NM_001164280.2:c.94T>C	NP_001157752.1:p.Ser32Pro
NM_001467.6:c.94T>C	NP_001458.1:p.Ser32Pro
NM_001164277.2:c.94T>C MANE Select	NP_001157749.1:p.Ser32Pro