Canonical Allele Identifier: CA382903665

Gene: SLC37A4

Linked Data

• dbSNP Id: rs1340404451
• MyVariant Identifiers: chr11:g.118898536G>A (hg19) ; chr11:g.119027826G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027826G>A , CM000673.2:g.119027826G>A	GRCh38
NC_000011.9:g.118898536G>A , CM000673.1:g.118898536G>A	GRCh37
NC_000011.8:g.118403746G>A	NCBI36
NG_013331.1:g.8081C>T , LRG_187:g.8081C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.657C>T
ENST00000697845.1:n.581C>T
ENST00000697846.1:n.657C>T
ENST00000697847.1:n.657C>T
ENST00000697848.1:n.657C>T
ENST00000697849.1:n.1696C>T
ENST00000697850.1:n.657C>T
ENST00000697851.1:n.2017C>T
ENST00000638186.1:n.731C>T
ENST00000638360.1:n.619-56C>T
ENST00000638925.1:n.664C>T
ENST00000650539.1:n.833C>T
ENST00000330775.9:c.428C>T	ENSP00000476242.2:p.Thr143Ile
ENST00000357590.9:c.428C>T	ENSP00000476176.2:p.Thr143Ile
ENST00000524428.5:n.749C>T
ENST00000525039.5:n.851C>T
ENST00000525102.5:n.1185C>T
ENST00000525372.5:n.428C>T
ENST00000525787.1:n.1044C>T
ENST00000526275.5:n.1209C>T
ENST00000526626.6:n.390C>T
ENST00000527992.5:n.655C>T
ENST00000529510.5:n.399+368C>T
ENST00000530407.5:n.577C>T
ENST00000532085.1:n.3038C>T
ENST00000532888.6:n.723C>T
ENST00000538950.5:c.209C>T	ENSP00000475991.2:p.Thr70Ile
ENST00000545985.5:c.428C>T	ENSP00000475241.2:p.Thr143Ile
NM_001164277.1:c.428C>T , LRG_187t1:c.428C>T	NP_001157749.1:p.Thr143Ile
NM_001164278.1:c.428C>T	NP_001157750.1:p.Thr143Ile
NM_001164279.1:c.209C>T	NP_001157751.1:p.Thr70Ile
NM_001164280.1:c.428C>T	NP_001157752.1:p.Thr143Ile
NM_001467.5:c.428C>T	NP_001458.1:p.Thr143Ile
NM_001164278.2:c.428C>T	NP_001157750.1:p.Thr143Ile
NM_001164279.2:c.209C>T	NP_001157751.1:p.Thr70Ile
NM_001164280.2:c.428C>T	NP_001157752.1:p.Thr143Ile
NM_001467.6:c.428C>T	NP_001458.1:p.Thr143Ile
NM_001164277.2:c.428C>T MANE Select	NP_001157749.1:p.Thr143Ile