Canonical Allele Identifier: CA477367800

Gene: SLC37A4

Linked Data

• MyVariant Identifiers: chr11:g.118898478G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027768G>A , CM000673.2:g.119027768G>A	GRCh38
NC_000011.9:g.118898478G>A , CM000673.1:g.118898478G>A	GRCh37
NC_000011.8:g.118403688G>A	NCBI36
NG_013331.1:g.8139C>T , LRG_187:g.8139C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.715C>T
ENST00000697845.1:n.639C>T
ENST00000697846.1:n.715C>T
ENST00000697847.1:n.715C>T
ENST00000697848.1:n.715C>T
ENST00000697849.1:n.1754C>T
ENST00000697850.1:n.715C>T
ENST00000697851.1:n.2075C>T
ENST00000638186.1:n.789C>T
ENST00000638360.1:n.621C>T
ENST00000638925.1:n.722C>T
ENST00000650539.1:n.891C>T
ENST00000330775.9:c.486C>T	ENSP00000476242.2:p.Ser162=
ENST00000357590.9:c.486C>T	ENSP00000476176.2:p.Ser162=
ENST00000524428.5:n.807C>T
ENST00000525039.5:n.909C>T
ENST00000525102.5:n.1243C>T
ENST00000525372.5:n.486C>T
ENST00000526275.5:n.1267C>T
ENST00000526626.6:n.448C>T
ENST00000527992.5:n.713C>T
ENST00000529510.5:n.399+426C>T
ENST00000530407.5:n.635C>T
ENST00000532085.1:n.3096C>T
ENST00000532888.6:n.781C>T
ENST00000538950.5:c.267C>T	ENSP00000475991.2:p.Ser89=
ENST00000545985.5:c.486C>T	ENSP00000475241.2:p.Ser162=
NM_001164277.1:c.486C>T , LRG_187t1:c.486C>T	NP_001157749.1:p.Ser162=
NM_001164278.1:c.486C>T	NP_001157750.1:p.Ser162=
NM_001164279.1:c.267C>T	NP_001157751.1:p.Ser89=
NM_001164280.1:c.486C>T	NP_001157752.1:p.Ser162=
NM_001467.5:c.486C>T	NP_001458.1:p.Ser162=
NM_001164278.2:c.486C>T	NP_001157750.1:p.Ser162=
NM_001164279.2:c.267C>T	NP_001157751.1:p.Ser89=
NM_001164280.2:c.486C>T	NP_001157752.1:p.Ser162=
NM_001467.6:c.486C>T	NP_001458.1:p.Ser162=
NM_001164277.2:c.486C>T MANE Select	NP_001157749.1:p.Ser162=