Canonical Allele Identifier: CA382894462

Gene: SLC37A4 TRAPPC4

Linked Data

• MyVariant Identifiers: chr11:g.118895743C>G (hg19) ; chr11:g.119025033C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025033C>G , CM000673.2:g.119025033C>G	GRCh38
NC_000011.9:g.118895743C>G , CM000673.1:g.118895743C>G	GRCh37
NC_000011.8:g.118400953C>G	NCBI36
NG_013331.1:g.10873G>C , LRG_187:g.10873G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.1377G>C (SLC37A4)
ENST00000697845.1:n.2366G>C (SLC37A4)
ENST00000697846.1:n.1739G>C (SLC37A4)
ENST00000697847.1:n.1450G>C (SLC37A4)
ENST00000697849.1:n.3843G>C (SLC37A4)
ENST00000697850.1:n.2034G>C (SLC37A4)
ENST00000697851.1:n.3005G>C (SLC37A4)
ENST00000638186.1:n.1471G>C (SLC37A4)
ENST00000638360.1:n.1303G>C (SLC37A4)
ENST00000638925.1:n.1436G>C (SLC37A4)
ENST00000650539.1:n.1639G>C (SLC37A4)
ENST00000330775.9:c.1167G>C (SLC37A4)	ENSP00000476242.2:p.Lys389Asn
ENST00000357590.9:c.1233G>C (SLC37A4)	ENSP00000476176.2:p.Lys411Asn
ENST00000524428.5:n.1403G>C (SLC37A4)
ENST00000525039.5:n.1657G>C (SLC37A4)
ENST00000525102.5:n.1925G>C (SLC37A4)
ENST00000525372.5:n.1265G>C (SLC37A4)
ENST00000526275.5:n.1949G>C (SLC37A4)
ENST00000527992.5:n.1395G>C (SLC37A4)
ENST00000530407.5:n.1317G>C (SLC37A4)
ENST00000532085.1:n.5185G>C (SLC37A4)
ENST00000533058.5:c.758C>G (TRAPPC4)	ENSP00000432920.1:p.Ala253Gly
ENST00000538950.5:c.948G>C (SLC37A4)	ENSP00000475991.2:p.Lys316Asn
ENST00000545985.5:c.1167G>C (SLC37A4)	ENSP00000475241.2:p.Lys389Asn
NM_001164277.1:c.1167G>C , LRG_187t1:c.1167G>C (SLC37A4)	NP_001157749.1:p.Lys389Asn
NM_001164278.1:c.1233G>C (SLC37A4)	NP_001157750.1:p.Lys411Asn
NM_001164279.1:c.948G>C (SLC37A4)	NP_001157751.1:p.Lys316Asn
NM_001164280.1:c.1167G>C (SLC37A4)	NP_001157752.1:p.Lys389Asn
NM_001467.5:c.1167G>C (SLC37A4)	NP_001458.1:p.Lys389Asn
NM_001164278.2:c.1233G>C (SLC37A4)	NP_001157750.1:p.Lys411Asn
NM_001164279.2:c.948G>C (SLC37A4)	NP_001157751.1:p.Lys316Asn
NM_001164280.2:c.1167G>C (SLC37A4)	NP_001157752.1:p.Lys389Asn
NM_001467.6:c.1167G>C (SLC37A4)	NP_001458.1:p.Lys389Asn
NM_001164277.2:c.1167G>C (SLC37A4) MANE Select	NP_001157749.1:p.Lys389Asn