Canonical Allele Identifier: CA477125125

Gene: SLC37A4

Linked Data

• MyVariant Identifiers: chr11:g.118896785T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026075T>G , CM000673.2:g.119026075T>G	GRCh38
NC_000011.9:g.118896785T>G , CM000673.1:g.118896785T>G	GRCh37
NC_000011.8:g.118401995T>G	NCBI36
NG_013331.1:g.9831A>C , LRG_187:g.9831A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1020A>C
ENST00000697845.1:n.1800A>C
ENST00000697846.1:n.1020A>C
ENST00000697847.1:n.1202-318A>C
ENST00000697848.1:n.1106A>C
ENST00000697849.1:n.2915A>C
ENST00000697850.1:n.1106A>C
ENST00000697851.1:n.2714A>C
ENST00000638186.1:n.1180A>C
ENST00000638360.1:n.1012A>C
ENST00000638925.1:n.1145A>C
ENST00000650539.1:n.1282A>C
ENST00000330775.9:c.876A>C	ENSP00000476242.2:p.Gly292=
ENST00000357590.9:c.876A>C	ENSP00000476176.2:p.Gly292=
ENST00000524428.5:n.1112A>C
ENST00000525039.5:n.1300A>C
ENST00000525102.5:n.1634A>C
ENST00000525372.5:n.974A>C
ENST00000526275.5:n.1658A>C
ENST00000527992.5:n.1104A>C
ENST00000529510.5:n.564A>C
ENST00000530407.5:n.1026A>C
ENST00000532085.1:n.4257A>C
ENST00000538950.5:c.657A>C	ENSP00000475991.2:p.Gly219=
ENST00000545985.5:c.876A>C	ENSP00000475241.2:p.Gly292=
NM_001164277.1:c.876A>C , LRG_187t1:c.876A>C	NP_001157749.1:p.Gly292=
NM_001164278.1:c.876A>C	NP_001157750.1:p.Gly292=
NM_001164279.1:c.657A>C	NP_001157751.1:p.Gly219=
NM_001164280.1:c.876A>C	NP_001157752.1:p.Gly292=
NM_001467.5:c.876A>C	NP_001458.1:p.Gly292=
NM_001164278.2:c.876A>C	NP_001157750.1:p.Gly292=
NM_001164279.2:c.657A>C	NP_001157751.1:p.Gly219=
NM_001164280.2:c.876A>C	NP_001157752.1:p.Gly292=
NM_001467.6:c.876A>C	NP_001458.1:p.Gly292=
NM_001164277.2:c.876A>C MANE Select	NP_001157749.1:p.Gly292=