Canonical Allele Identifier: CA382894736

Gene: SLC37A4 TRAPPC4

Linked Data

• MyVariant Identifiers: chr11:g.118895763G>C (hg19) ; chr11:g.119025053G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025053G>C , CM000673.2:g.119025053G>C	GRCh38
NC_000011.9:g.118895763G>C , CM000673.1:g.118895763G>C	GRCh37
NC_000011.8:g.118400973G>C	NCBI36
NG_013331.1:g.10853C>G , LRG_187:g.10853C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.1357C>G (SLC37A4)
ENST00000697845.1:n.2346C>G (SLC37A4)
ENST00000697846.1:n.1719C>G (SLC37A4)
ENST00000697847.1:n.1430C>G (SLC37A4)
ENST00000697849.1:n.3823C>G (SLC37A4)
ENST00000697850.1:n.2014C>G (SLC37A4)
ENST00000697851.1:n.2985C>G (SLC37A4)
ENST00000638186.1:n.1451C>G (SLC37A4)
ENST00000638360.1:n.1283C>G (SLC37A4)
ENST00000638925.1:n.1416C>G (SLC37A4)
ENST00000650539.1:n.1619C>G (SLC37A4)
ENST00000330775.9:c.1147C>G (SLC37A4)	ENSP00000476242.2:p.Pro383Ala
ENST00000357590.9:c.1213C>G (SLC37A4)	ENSP00000476176.2:p.Pro405Ala
ENST00000524428.5:n.1383C>G (SLC37A4)
ENST00000525039.5:n.1637C>G (SLC37A4)
ENST00000525102.5:n.1905C>G (SLC37A4)
ENST00000525372.5:n.1245C>G (SLC37A4)
ENST00000526275.5:n.1929C>G (SLC37A4)
ENST00000527992.5:n.1375C>G (SLC37A4)
ENST00000530407.5:n.1297C>G (SLC37A4)
ENST00000532085.1:n.5165C>G (SLC37A4)
ENST00000533058.5:c.*4G>C (TRAPPC4)	ENSP00000432920.1:n.*4G>C
ENST00000538950.5:c.928C>G (SLC37A4)	ENSP00000475991.2:p.Pro310Ala
ENST00000545985.5:c.1147C>G (SLC37A4)	ENSP00000475241.2:p.Pro383Ala
NM_001164277.1:c.1147C>G , LRG_187t1:c.1147C>G (SLC37A4)	NP_001157749.1:p.Pro383Ala
NM_001164278.1:c.1213C>G (SLC37A4)	NP_001157750.1:p.Pro405Ala
NM_001164279.1:c.928C>G (SLC37A4)	NP_001157751.1:p.Pro310Ala
NM_001164280.1:c.1147C>G (SLC37A4)	NP_001157752.1:p.Pro383Ala
NM_001467.5:c.1147C>G (SLC37A4)	NP_001458.1:p.Pro383Ala
NM_001164278.2:c.1213C>G (SLC37A4)	NP_001157750.1:p.Pro405Ala
NM_001164279.2:c.928C>G (SLC37A4)	NP_001157751.1:p.Pro310Ala
NM_001164280.2:c.1147C>G (SLC37A4)	NP_001157752.1:p.Pro383Ala
NM_001467.6:c.1147C>G (SLC37A4)	NP_001458.1:p.Pro383Ala
NM_001164277.2:c.1147C>G (SLC37A4) MANE Select	NP_001157749.1:p.Pro383Ala