Canonical Allele Identifier: CA382902956

Gene: SLC37A4

Linked Data

• gnomAD v4: 11-119027763-C-G
• MyVariant Identifiers: chr11:g.118898473C>G (hg19) ; chr11:g.119027763C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027763C>G , CM000673.2:g.119027763C>G	GRCh38
NC_000011.9:g.118898473C>G , CM000673.1:g.118898473C>G	GRCh37
NC_000011.8:g.118403683C>G	NCBI36
NG_013331.1:g.8144G>C , LRG_187:g.8144G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.720G>C
ENST00000697845.1:n.644G>C
ENST00000697846.1:n.720G>C
ENST00000697847.1:n.720G>C
ENST00000697848.1:n.720G>C
ENST00000697849.1:n.1759G>C
ENST00000697850.1:n.720G>C
ENST00000697851.1:n.2080G>C
ENST00000638186.1:n.794G>C
ENST00000638360.1:n.626G>C
ENST00000638925.1:n.727G>C
ENST00000650539.1:n.896G>C
ENST00000330775.9:c.491G>C	ENSP00000476242.2:p.Ser164Thr
ENST00000357590.9:c.491G>C	ENSP00000476176.2:p.Ser164Thr
ENST00000524428.5:n.812G>C
ENST00000525039.5:n.914G>C
ENST00000525102.5:n.1248G>C
ENST00000525372.5:n.491G>C
ENST00000526275.5:n.1272G>C
ENST00000526626.6:n.453G>C
ENST00000527992.5:n.718G>C
ENST00000529510.5:n.399+431G>C
ENST00000530407.5:n.640G>C
ENST00000532085.1:n.3101G>C
ENST00000532888.6:n.786G>C
ENST00000538950.5:c.272G>C	ENSP00000475991.2:p.Ser91Thr
ENST00000545985.5:c.491G>C	ENSP00000475241.2:p.Ser164Thr
NM_001164277.1:c.491G>C , LRG_187t1:c.491G>C	NP_001157749.1:p.Ser164Thr
NM_001164278.1:c.491G>C	NP_001157750.1:p.Ser164Thr
NM_001164279.1:c.272G>C	NP_001157751.1:p.Ser91Thr
NM_001164280.1:c.491G>C	NP_001157752.1:p.Ser164Thr
NM_001467.5:c.491G>C	NP_001458.1:p.Ser164Thr
NM_001164278.2:c.491G>C	NP_001157750.1:p.Ser164Thr
NM_001164279.2:c.272G>C	NP_001157751.1:p.Ser91Thr
NM_001164280.2:c.491G>C	NP_001157752.1:p.Ser164Thr
NM_001467.6:c.491G>C	NP_001458.1:p.Ser164Thr
NM_001164277.2:c.491G>C MANE Select	NP_001157749.1:p.Ser164Thr