Canonical Allele Identifier: CA477124942

Gene: SLC37A4

Linked Data

• MyVariant Identifiers: chr11:g.118896683G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025973G>C , CM000673.2:g.119025973G>C	GRCh38
NC_000011.9:g.118896683G>C , CM000673.1:g.118896683G>C	GRCh37
NC_000011.8:g.118401893G>C	NCBI36
NG_013331.1:g.9933C>G , LRG_187:g.9933C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1122C>G
ENST00000697845.1:n.1902C>G
ENST00000697846.1:n.1122C>G
ENST00000697847.1:n.1202-216C>G
ENST00000697848.1:n.1208C>G
ENST00000697849.1:n.3017C>G
ENST00000697850.1:n.1208C>G
ENST00000697851.1:n.2816C>G
ENST00000638186.1:n.1282C>G
ENST00000638360.1:n.1114C>G
ENST00000638925.1:n.1247C>G
ENST00000650539.1:n.1384C>G
ENST00000330775.9:c.978C>G	ENSP00000476242.2:p.Ser326=
ENST00000357590.9:c.978C>G	ENSP00000476176.2:p.Ser326=
ENST00000524428.5:n.1214C>G
ENST00000525039.5:n.1402C>G
ENST00000525102.5:n.1736C>G
ENST00000525372.5:n.1076C>G
ENST00000526275.5:n.1760C>G
ENST00000527992.5:n.1206C>G
ENST00000529510.5:n.666C>G
ENST00000530407.5:n.1128C>G
ENST00000532085.1:n.4359C>G
ENST00000538950.5:c.759C>G	ENSP00000475991.2:p.Ser253=
ENST00000545985.5:c.978C>G	ENSP00000475241.2:p.Ser326=
NM_001164277.1:c.978C>G , LRG_187t1:c.978C>G	NP_001157749.1:p.Ser326=
NM_001164278.1:c.978C>G	NP_001157750.1:p.Ser326=
NM_001164279.1:c.759C>G	NP_001157751.1:p.Ser253=
NM_001164280.1:c.978C>G	NP_001157752.1:p.Ser326=
NM_001467.5:c.978C>G	NP_001458.1:p.Ser326=
NM_001164278.2:c.978C>G	NP_001157750.1:p.Ser326=
NM_001164279.2:c.759C>G	NP_001157751.1:p.Ser253=
NM_001164280.2:c.978C>G	NP_001157752.1:p.Ser326=
NM_001467.6:c.978C>G	NP_001458.1:p.Ser326=
NM_001164277.2:c.978C>G MANE Select	NP_001157749.1:p.Ser326=