Canonical Allele Identifier: CA477367872

Gene: SLC37A4

Linked Data

• MyVariant Identifiers: chr11:g.118898526G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027816G>A , CM000673.2:g.119027816G>A	GRCh38
NC_000011.9:g.118898526G>A , CM000673.1:g.118898526G>A	GRCh37
NC_000011.8:g.118403736G>A	NCBI36
NG_013331.1:g.8091C>T , LRG_187:g.8091C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.667C>T
ENST00000697845.1:n.591C>T
ENST00000697846.1:n.667C>T
ENST00000697847.1:n.667C>T
ENST00000697848.1:n.667C>T
ENST00000697849.1:n.1706C>T
ENST00000697850.1:n.667C>T
ENST00000697851.1:n.2027C>T
ENST00000638186.1:n.741C>T
ENST00000638360.1:n.619-46C>T
ENST00000638925.1:n.674C>T
ENST00000650539.1:n.843C>T
ENST00000330775.9:c.438C>T	ENSP00000476242.2:p.Asn146=
ENST00000357590.9:c.438C>T	ENSP00000476176.2:p.Asn146=
ENST00000524428.5:n.759C>T
ENST00000525039.5:n.861C>T
ENST00000525102.5:n.1195C>T
ENST00000525372.5:n.438C>T
ENST00000525787.1:n.1054C>T
ENST00000526275.5:n.1219C>T
ENST00000526626.6:n.400C>T
ENST00000527992.5:n.665C>T
ENST00000529510.5:n.399+378C>T
ENST00000530407.5:n.587C>T
ENST00000532085.1:n.3048C>T
ENST00000532888.6:n.733C>T
ENST00000538950.5:c.219C>T	ENSP00000475991.2:p.Asn73=
ENST00000545985.5:c.438C>T	ENSP00000475241.2:p.Asn146=
NM_001164277.1:c.438C>T , LRG_187t1:c.438C>T	NP_001157749.1:p.Asn146=
NM_001164278.1:c.438C>T	NP_001157750.1:p.Asn146=
NM_001164279.1:c.219C>T	NP_001157751.1:p.Asn73=
NM_001164280.1:c.438C>T	NP_001157752.1:p.Asn146=
NM_001467.5:c.438C>T	NP_001458.1:p.Asn146=
NM_001164278.2:c.438C>T	NP_001157750.1:p.Asn146=
NM_001164279.2:c.219C>T	NP_001157751.1:p.Asn73=
NM_001164280.2:c.438C>T	NP_001157752.1:p.Asn146=
NM_001467.6:c.438C>T	NP_001458.1:p.Asn146=
NM_001164277.2:c.438C>T MANE Select	NP_001157749.1:p.Asn146=