Canonical Allele Identifier: CA2616339369

Gene: SLC37A4 TRAPPC4

Linked Data

• gnomAD v4: 11-119024690-GAGTCTA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119024693_119024698del , CM000673.2:g.119024693_119024698del	GRCh38
NC_000011.9:g.118895403_118895408del , CM000673.1:g.118895403_118895408del	GRCh37
NC_000011.8:g.118400613_118400618del	NCBI36
NG_013331.1:g.11210_11215del , LRG_187:g.11210_11215del

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.1714_1719del (SLC37A4)
ENST00000697845.1:n.2703_2708del (SLC37A4)
ENST00000697846.1:n.2076_2081del (SLC37A4)
ENST00000697847.1:n.1787_1792del (SLC37A4)
ENST00000697849.1:n.4180_4185del (SLC37A4)
ENST00000697850.1:n.2371_2376del (SLC37A4)
ENST00000697851.1:n.3342_3347del (SLC37A4)
ENST00000638186.1:n.1808_1813del (SLC37A4)
ENST00000638360.1:n.1640_1645del (SLC37A4)
ENST00000638925.1:n.1773_1778del (SLC37A4)
ENST00000650539.1:n.1976_1981del (SLC37A4)
ENST00000330775.9:c.*214_*219del (SLC37A4)	ENSP00000476242.2:n.*214_*219del
ENST00000357590.9:c.*214_*219del (SLC37A4)	ENSP00000476176.2:n.*214_*219del
ENST00000525102.5:n.2262_2267del (SLC37A4)
ENST00000526275.5:n.2286_2291del (SLC37A4)
ENST00000527992.5:n.1732_1737del (SLC37A4)
ENST00000532085.1:n.5522_5527del (SLC37A4)
ENST00000533058.5:c.582-164_582-159del (TRAPPC4)	ENSP00000432920.1:n.582-164_582-159del
ENST00000538950.5:c.*214_*219del (SLC37A4)	ENSP00000475991.2:n.*214_*219del
ENST00000545985.5:c.*214_*219del (SLC37A4)	ENSP00000475241.2:n.*214_*219del
NM_001164277.1:c.*214_*219del , LRG_187t1:c.*214_*219del (SLC37A4)	NP_001157749.1:n.*214_*219del
NM_001164278.1:c.*214_*219del (SLC37A4)	NP_001157750.1:n.*214_*219del
NM_001164279.1:c.*214_*219del (SLC37A4)	NP_001157751.1:n.*214_*219del
NM_001164280.1:c.*214_*219del (SLC37A4)	NP_001157752.1:n.*214_*219del
NM_001467.5:c.*214_*219del (SLC37A4)	NP_001458.1:n.*214_*219del
NM_001164278.2:c.*214_*219del (SLC37A4)	NP_001157750.1:n.*214_*219del
NM_001164279.2:c.*214_*219del (SLC37A4)	NP_001157751.1:n.*214_*219del
NM_001164280.2:c.*214_*219del (SLC37A4)	NP_001157752.1:n.*214_*219del
NM_001467.6:c.*214_*219del (SLC37A4)	NP_001458.1:n.*214_*219del
NM_001164277.2:c.*214_*219del (SLC37A4) MANE Select	NP_001157749.1:n.*214_*219del