Canonical Allele Identifier: CA382896394

Gene: SLC37A4 TRAPPC4

Linked Data

• MyVariant Identifiers: chr11:g.118896027C>A (hg19) ; chr11:g.119025317C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025317C>A , CM000673.2:g.119025317C>A	GRCh38
NC_000011.9:g.118896027C>A , CM000673.1:g.118896027C>A	GRCh37
NC_000011.8:g.118401237C>A	NCBI36
NG_013331.1:g.10589G>T , LRG_187:g.10589G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1207G>T (SLC37A4)
ENST00000697845.1:n.2196G>T (SLC37A4)
ENST00000697846.1:n.1569G>T (SLC37A4)
ENST00000697847.1:n.1280G>T (SLC37A4)
ENST00000697849.1:n.3673G>T (SLC37A4)
ENST00000697850.1:n.1864G>T (SLC37A4)
ENST00000697851.1:n.2835G>T (SLC37A4)
ENST00000638186.1:n.1301G>T (SLC37A4)
ENST00000638360.1:n.1133G>T (SLC37A4)
ENST00000638925.1:n.1266G>T (SLC37A4)
ENST00000650539.1:n.1469G>T (SLC37A4)
ENST00000330775.9:c.997G>T (SLC37A4)	ENSP00000476242.2:p.Val333Leu
ENST00000357590.9:c.1063G>T (SLC37A4)	ENSP00000476176.2:p.Val355Leu
ENST00000524428.5:n.1233G>T (SLC37A4)
ENST00000525039.5:n.1487G>T (SLC37A4)
ENST00000525102.5:n.1755G>T (SLC37A4)
ENST00000525372.5:n.1095G>T (SLC37A4)
ENST00000526275.5:n.1779G>T (SLC37A4)
ENST00000527992.5:n.1225G>T (SLC37A4)
ENST00000529510.5:n.685G>T (SLC37A4)
ENST00000530407.5:n.1147G>T (SLC37A4)
ENST00000532085.1:n.5015G>T (SLC37A4)
ENST00000533058.5:c.*268C>A (TRAPPC4)	ENSP00000432920.1:n.*268C>A
ENST00000538950.5:c.778G>T (SLC37A4)	ENSP00000475991.2:p.Val260Leu
ENST00000545985.5:c.997G>T (SLC37A4)	ENSP00000475241.2:p.Val333Leu
NM_001164277.1:c.997G>T , LRG_187t1:c.997G>T (SLC37A4)	NP_001157749.1:p.Val333Leu
NM_001164278.1:c.1063G>T (SLC37A4)	NP_001157750.1:p.Val355Leu
NM_001164279.1:c.778G>T (SLC37A4)	NP_001157751.1:p.Val260Leu
NM_001164280.1:c.997G>T (SLC37A4)	NP_001157752.1:p.Val333Leu
NM_001467.5:c.997G>T (SLC37A4)	NP_001458.1:p.Val333Leu
NM_001164278.2:c.1063G>T (SLC37A4)	NP_001157750.1:p.Val355Leu
NM_001164279.2:c.778G>T (SLC37A4)	NP_001157751.1:p.Val260Leu
NM_001164280.2:c.997G>T (SLC37A4)	NP_001157752.1:p.Val333Leu
NM_001467.6:c.997G>T (SLC37A4)	NP_001458.1:p.Val333Leu
NM_001164277.2:c.997G>T (SLC37A4) MANE Select	NP_001157749.1:p.Val333Leu