Canonical Allele Identifier: CA2616339443

Gene: SLC37A4 TRAPPC4

Linked Data

• gnomAD v4: 11-119024763-ACTTCCAGCG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119024765_119024773del , CM000673.2:g.119024765_119024773del	GRCh38
NC_000011.9:g.118895475_118895483del , CM000673.1:g.118895475_118895483del	GRCh37
NC_000011.8:g.118400685_118400693del	NCBI36
NG_013331.1:g.11134_11142del , LRG_187:g.11134_11142del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1638_1646del (SLC37A4)
ENST00000697845.1:n.2627_2635del (SLC37A4)
ENST00000697846.1:n.2000_2008del (SLC37A4)
ENST00000697847.1:n.1711_1719del (SLC37A4)
ENST00000697849.1:n.4104_4112del (SLC37A4)
ENST00000697850.1:n.2295_2303del (SLC37A4)
ENST00000697851.1:n.3266_3274del (SLC37A4)
ENST00000638186.1:n.1732_1740del (SLC37A4)
ENST00000638360.1:n.1564_1572del (SLC37A4)
ENST00000638925.1:n.1697_1705del (SLC37A4)
ENST00000650539.1:n.1900_1908del (SLC37A4)
ENST00000330775.9:c.*138_*146del (SLC37A4)	ENSP00000476242.2:n.*138_*146del
ENST00000357590.9:c.*138_*146del (SLC37A4)	ENSP00000476176.2:n.*138_*146del
ENST00000525102.5:n.2186_2194del (SLC37A4)
ENST00000526275.5:n.2210_2218del (SLC37A4)
ENST00000527992.5:n.1656_1664del (SLC37A4)
ENST00000532085.1:n.5446_5454del (SLC37A4)
ENST00000533058.5:c.582-92_582-84del (TRAPPC4)	ENSP00000432920.1:n.582-92_582-84del
ENST00000538950.5:c.*138_*146del (SLC37A4)	ENSP00000475991.2:n.*138_*146del
ENST00000545985.5:c.*138_*146del (SLC37A4)	ENSP00000475241.2:n.*138_*146del
NM_001164277.1:c.*138_*146del , LRG_187t1:c.*138_*146del (SLC37A4)	NP_001157749.1:n.*138_*146del
NM_001164278.1:c.*138_*146del (SLC37A4)	NP_001157750.1:n.*138_*146del
NM_001164279.1:c.*138_*146del (SLC37A4)	NP_001157751.1:n.*138_*146del
NM_001164280.1:c.*138_*146del (SLC37A4)	NP_001157752.1:n.*138_*146del
NM_001467.5:c.*138_*146del (SLC37A4)	NP_001458.1:n.*138_*146del
NM_001164278.2:c.*138_*146del (SLC37A4)	NP_001157750.1:n.*138_*146del
NM_001164279.2:c.*138_*146del (SLC37A4)	NP_001157751.1:n.*138_*146del
NM_001164280.2:c.*138_*146del (SLC37A4)	NP_001157752.1:n.*138_*146del
NM_001467.6:c.*138_*146del (SLC37A4)	NP_001458.1:n.*138_*146del
NM_001164277.2:c.*138_*146del (SLC37A4) MANE Select	NP_001157749.1:n.*138_*146del