Canonical Allele Identifier: CA382896405

Gene: SLC37A4 TRAPPC4

Linked Data

• MyVariant Identifiers: chr11:g.118896030G>C (hg19) ; chr11:g.119025320G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025320G>C , CM000673.2:g.119025320G>C	GRCh38
NC_000011.9:g.118896030G>C , CM000673.1:g.118896030G>C	GRCh37
NC_000011.8:g.118401240G>C	NCBI36
NG_013331.1:g.10586C>G , LRG_187:g.10586C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1204C>G (SLC37A4)
ENST00000697845.1:n.2193C>G (SLC37A4)
ENST00000697846.1:n.1566C>G (SLC37A4)
ENST00000697847.1:n.1277C>G (SLC37A4)
ENST00000697849.1:n.3670C>G (SLC37A4)
ENST00000697850.1:n.1861C>G (SLC37A4)
ENST00000697851.1:n.2832C>G (SLC37A4)
ENST00000638186.1:n.1298C>G (SLC37A4)
ENST00000638360.1:n.1130C>G (SLC37A4)
ENST00000638925.1:n.1263C>G (SLC37A4)
ENST00000650539.1:n.1466C>G (SLC37A4)
ENST00000330775.9:c.994C>G (SLC37A4)	ENSP00000476242.2:p.Leu332Val
ENST00000357590.9:c.1060C>G (SLC37A4)	ENSP00000476176.2:p.Leu354Val
ENST00000524428.5:n.1230C>G (SLC37A4)
ENST00000525039.5:n.1484C>G (SLC37A4)
ENST00000525102.5:n.1752C>G (SLC37A4)
ENST00000525372.5:n.1092C>G (SLC37A4)
ENST00000526275.5:n.1776C>G (SLC37A4)
ENST00000527992.5:n.1222C>G (SLC37A4)
ENST00000529510.5:n.682C>G (SLC37A4)
ENST00000530407.5:n.1144C>G (SLC37A4)
ENST00000532085.1:n.5012C>G (SLC37A4)
ENST00000533058.5:c.*271G>C (TRAPPC4)	ENSP00000432920.1:n.*271G>C
ENST00000538950.5:c.775C>G (SLC37A4)	ENSP00000475991.2:p.Leu259Val
ENST00000545985.5:c.994C>G (SLC37A4)	ENSP00000475241.2:p.Leu332Val
NM_001164277.1:c.994C>G , LRG_187t1:c.994C>G (SLC37A4)	NP_001157749.1:p.Leu332Val
NM_001164278.1:c.1060C>G (SLC37A4)	NP_001157750.1:p.Leu354Val
NM_001164279.1:c.775C>G (SLC37A4)	NP_001157751.1:p.Leu259Val
NM_001164280.1:c.994C>G (SLC37A4)	NP_001157752.1:p.Leu332Val
NM_001467.5:c.994C>G (SLC37A4)	NP_001458.1:p.Leu332Val
NM_001164278.2:c.1060C>G (SLC37A4)	NP_001157750.1:p.Leu354Val
NM_001164279.2:c.775C>G (SLC37A4)	NP_001157751.1:p.Leu259Val
NM_001164280.2:c.994C>G (SLC37A4)	NP_001157752.1:p.Leu332Val
NM_001467.6:c.994C>G (SLC37A4)	NP_001458.1:p.Leu332Val
NM_001164277.2:c.994C>G (SLC37A4) MANE Select	NP_001157749.1:p.Leu332Val