Canonical Allele Identifier: CA477124961

Gene: SLC37A4

Linked Data

• MyVariant Identifiers: chr11:g.118896706G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025996G>T , CM000673.2:g.119025996G>T	GRCh38
NC_000011.9:g.118896706G>T , CM000673.1:g.118896706G>T	GRCh37
NC_000011.8:g.118401916G>T	NCBI36
NG_013331.1:g.9910C>A , LRG_187:g.9910C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1099C>A
ENST00000697845.1:n.1879C>A
ENST00000697846.1:n.1099C>A
ENST00000697847.1:n.1202-239C>A
ENST00000697848.1:n.1185C>A
ENST00000697849.1:n.2994C>A
ENST00000697850.1:n.1185C>A
ENST00000697851.1:n.2793C>A
ENST00000638186.1:n.1259C>A
ENST00000638360.1:n.1091C>A
ENST00000638925.1:n.1224C>A
ENST00000650539.1:n.1361C>A
ENST00000330775.9:c.955C>A	ENSP00000476242.2:p.Arg319=
ENST00000357590.9:c.955C>A	ENSP00000476176.2:p.Arg319=
ENST00000524428.5:n.1191C>A
ENST00000525039.5:n.1379C>A
ENST00000525102.5:n.1713C>A
ENST00000525372.5:n.1053C>A
ENST00000526275.5:n.1737C>A
ENST00000527992.5:n.1183C>A
ENST00000529510.5:n.643C>A
ENST00000530407.5:n.1105C>A
ENST00000532085.1:n.4336C>A
ENST00000538950.5:c.736C>A	ENSP00000475991.2:p.Arg246=
ENST00000545985.5:c.955C>A	ENSP00000475241.2:p.Arg319=
NM_001164277.1:c.955C>A , LRG_187t1:c.955C>A	NP_001157749.1:p.Arg319=
NM_001164278.1:c.955C>A	NP_001157750.1:p.Arg319=
NM_001164279.1:c.736C>A	NP_001157751.1:p.Arg246=
NM_001164280.1:c.955C>A	NP_001157752.1:p.Arg319=
NM_001467.5:c.955C>A	NP_001458.1:p.Arg319=
NM_001164278.2:c.955C>A	NP_001157750.1:p.Arg319=
NM_001164279.2:c.736C>A	NP_001157751.1:p.Arg246=
NM_001164280.2:c.955C>A	NP_001157752.1:p.Arg319=
NM_001467.6:c.955C>A	NP_001458.1:p.Arg319=
NM_001164277.2:c.955C>A MANE Select	NP_001157749.1:p.Arg319=