Canonical Allele Identifier: CA382896403

Gene: SLC37A4 TRAPPC4

Linked Data

• MyVariant Identifiers: chr11:g.118896029A>G (hg19) ; chr11:g.119025319A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025319A>G , CM000673.2:g.119025319A>G	GRCh38
NC_000011.9:g.118896029A>G , CM000673.1:g.118896029A>G	GRCh37
NC_000011.8:g.118401239A>G	NCBI36
NG_013331.1:g.10587T>C , LRG_187:g.10587T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1205T>C (SLC37A4)
ENST00000697845.1:n.2194T>C (SLC37A4)
ENST00000697846.1:n.1567T>C (SLC37A4)
ENST00000697847.1:n.1278T>C (SLC37A4)
ENST00000697849.1:n.3671T>C (SLC37A4)
ENST00000697850.1:n.1862T>C (SLC37A4)
ENST00000697851.1:n.2833T>C (SLC37A4)
ENST00000638186.1:n.1299T>C (SLC37A4)
ENST00000638360.1:n.1131T>C (SLC37A4)
ENST00000638925.1:n.1264T>C (SLC37A4)
ENST00000650539.1:n.1467T>C (SLC37A4)
ENST00000330775.9:c.995T>C (SLC37A4)	ENSP00000476242.2:p.Leu332Pro
ENST00000357590.9:c.1061T>C (SLC37A4)	ENSP00000476176.2:p.Leu354Pro
ENST00000524428.5:n.1231T>C (SLC37A4)
ENST00000525039.5:n.1485T>C (SLC37A4)
ENST00000525102.5:n.1753T>C (SLC37A4)
ENST00000525372.5:n.1093T>C (SLC37A4)
ENST00000526275.5:n.1777T>C (SLC37A4)
ENST00000527992.5:n.1223T>C (SLC37A4)
ENST00000529510.5:n.683T>C (SLC37A4)
ENST00000530407.5:n.1145T>C (SLC37A4)
ENST00000532085.1:n.5013T>C (SLC37A4)
ENST00000533058.5:c.*270A>G (TRAPPC4)	ENSP00000432920.1:n.*270A>G
ENST00000538950.5:c.776T>C (SLC37A4)	ENSP00000475991.2:p.Leu259Pro
ENST00000545985.5:c.995T>C (SLC37A4)	ENSP00000475241.2:p.Leu332Pro
NM_001164277.1:c.995T>C , LRG_187t1:c.995T>C (SLC37A4)	NP_001157749.1:p.Leu332Pro
NM_001164278.1:c.1061T>C (SLC37A4)	NP_001157750.1:p.Leu354Pro
NM_001164279.1:c.776T>C (SLC37A4)	NP_001157751.1:p.Leu259Pro
NM_001164280.1:c.995T>C (SLC37A4)	NP_001157752.1:p.Leu332Pro
NM_001467.5:c.995T>C (SLC37A4)	NP_001458.1:p.Leu332Pro
NM_001164278.2:c.1061T>C (SLC37A4)	NP_001157750.1:p.Leu354Pro
NM_001164279.2:c.776T>C (SLC37A4)	NP_001157751.1:p.Leu259Pro
NM_001164280.2:c.995T>C (SLC37A4)	NP_001157752.1:p.Leu332Pro
NM_001467.6:c.995T>C (SLC37A4)	NP_001458.1:p.Leu332Pro
NM_001164277.2:c.995T>C (SLC37A4) MANE Select	NP_001157749.1:p.Leu332Pro