Canonical Allele Identifier: CA382896063

Gene: SLC37A4 TRAPPC4

Linked Data

• MyVariant Identifiers: chr11:g.118895990G>C (hg19) ; chr11:g.119025280G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025280G>C , CM000673.2:g.119025280G>C	GRCh38
NC_000011.9:g.118895990G>C , CM000673.1:g.118895990G>C	GRCh37
NC_000011.8:g.118401200G>C	NCBI36
NG_013331.1:g.10626C>G , LRG_187:g.10626C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.1244C>G (SLC37A4)
ENST00000697845.1:n.2233C>G (SLC37A4)
ENST00000697846.1:n.1606C>G (SLC37A4)
ENST00000697847.1:n.1317C>G (SLC37A4)
ENST00000697849.1:n.3710C>G (SLC37A4)
ENST00000697850.1:n.1901C>G (SLC37A4)
ENST00000697851.1:n.2872C>G (SLC37A4)
ENST00000638186.1:n.1338C>G (SLC37A4)
ENST00000638360.1:n.1170C>G (SLC37A4)
ENST00000638925.1:n.1303C>G (SLC37A4)
ENST00000650539.1:n.1506C>G (SLC37A4)
ENST00000330775.9:c.1034C>G (SLC37A4)	ENSP00000476242.2:p.Pro345Arg
ENST00000357590.9:c.1100C>G (SLC37A4)	ENSP00000476176.2:p.Pro367Arg
ENST00000524428.5:n.1270C>G (SLC37A4)
ENST00000525039.5:n.1524C>G (SLC37A4)
ENST00000525102.5:n.1792C>G (SLC37A4)
ENST00000525372.5:n.1132C>G (SLC37A4)
ENST00000526275.5:n.1816C>G (SLC37A4)
ENST00000527992.5:n.1262C>G (SLC37A4)
ENST00000529510.5:n.722C>G (SLC37A4)
ENST00000530407.5:n.1184C>G (SLC37A4)
ENST00000532085.1:n.5052C>G (SLC37A4)
ENST00000533058.5:c.*231G>C (TRAPPC4)	ENSP00000432920.1:n.*231G>C
ENST00000538950.5:c.815C>G (SLC37A4)	ENSP00000475991.2:p.Pro272Arg
ENST00000545985.5:c.1034C>G (SLC37A4)	ENSP00000475241.2:p.Pro345Arg
NM_001164277.1:c.1034C>G , LRG_187t1:c.1034C>G (SLC37A4)	NP_001157749.1:p.Pro345Arg
NM_001164278.1:c.1100C>G (SLC37A4)	NP_001157750.1:p.Pro367Arg
NM_001164279.1:c.815C>G (SLC37A4)	NP_001157751.1:p.Pro272Arg
NM_001164280.1:c.1034C>G (SLC37A4)	NP_001157752.1:p.Pro345Arg
NM_001467.5:c.1034C>G (SLC37A4)	NP_001458.1:p.Pro345Arg
NM_001164278.2:c.1100C>G (SLC37A4)	NP_001157750.1:p.Pro367Arg
NM_001164279.2:c.815C>G (SLC37A4)	NP_001157751.1:p.Pro272Arg
NM_001164280.2:c.1034C>G (SLC37A4)	NP_001157752.1:p.Pro345Arg
NM_001467.6:c.1034C>G (SLC37A4)	NP_001458.1:p.Pro345Arg
NM_001164277.2:c.1034C>G (SLC37A4) MANE Select	NP_001157749.1:p.Pro345Arg