Canonical Allele Identifier: CA382895409

Gene: SLC37A4 TRAPPC4

Linked Data

• gnomAD v4: 11-119025216-G-T
• MyVariant Identifiers: chr11:g.118895926G>T (hg19) ; chr11:g.119025216G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025216G>T , CM000673.2:g.119025216G>T	GRCh38
NC_000011.9:g.118895926G>T , CM000673.1:g.118895926G>T	GRCh37
NC_000011.8:g.118401136G>T	NCBI36
NG_013331.1:g.10690C>A , LRG_187:g.10690C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1308C>A (SLC37A4)
ENST00000697845.1:n.2297C>A (SLC37A4)
ENST00000697846.1:n.1670C>A (SLC37A4)
ENST00000697847.1:n.1381C>A (SLC37A4)
ENST00000697849.1:n.3774C>A (SLC37A4)
ENST00000697850.1:n.1965C>A (SLC37A4)
ENST00000697851.1:n.2936C>A (SLC37A4)
ENST00000638186.1:n.1402C>A (SLC37A4)
ENST00000638360.1:n.1234C>A (SLC37A4)
ENST00000638925.1:n.1367C>A (SLC37A4)
ENST00000650539.1:n.1570C>A (SLC37A4)
ENST00000330775.9:c.1098C>A (SLC37A4)	ENSP00000476242.2:p.His366Gln
ENST00000357590.9:c.1164C>A (SLC37A4)	ENSP00000476176.2:p.His388Gln
ENST00000524428.5:n.1334C>A (SLC37A4)
ENST00000525039.5:n.1588C>A (SLC37A4)
ENST00000525102.5:n.1856C>A (SLC37A4)
ENST00000525372.5:n.1196C>A (SLC37A4)
ENST00000526275.5:n.1880C>A (SLC37A4)
ENST00000527992.5:n.1326C>A (SLC37A4)
ENST00000529510.5:n.786C>A (SLC37A4)
ENST00000530407.5:n.1248C>A (SLC37A4)
ENST00000532085.1:n.5116C>A (SLC37A4)
ENST00000533058.5:c.*167G>T (TRAPPC4)	ENSP00000432920.1:n.*167G>T
ENST00000538950.5:c.879C>A (SLC37A4)	ENSP00000475991.2:p.His293Gln
ENST00000545985.5:c.1098C>A (SLC37A4)	ENSP00000475241.2:p.His366Gln
NM_001164277.1:c.1098C>A , LRG_187t1:c.1098C>A (SLC37A4)	NP_001157749.1:p.His366Gln
NM_001164278.1:c.1164C>A (SLC37A4)	NP_001157750.1:p.His388Gln
NM_001164279.1:c.879C>A (SLC37A4)	NP_001157751.1:p.His293Gln
NM_001164280.1:c.1098C>A (SLC37A4)	NP_001157752.1:p.His366Gln
NM_001467.5:c.1098C>A (SLC37A4)	NP_001458.1:p.His366Gln
NM_001164278.2:c.1164C>A (SLC37A4)	NP_001157750.1:p.His388Gln
NM_001164279.2:c.879C>A (SLC37A4)	NP_001157751.1:p.His293Gln
NM_001164280.2:c.1098C>A (SLC37A4)	NP_001157752.1:p.His366Gln
NM_001467.6:c.1098C>A (SLC37A4)	NP_001458.1:p.His366Gln
NM_001164277.2:c.1098C>A (SLC37A4) MANE Select	NP_001157749.1:p.His366Gln