Canonical Allele Identifier: CA2616334843

Gene: SLC37A4

Linked Data

• gnomAD v4: 11-119026707-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026708del , CM000673.2:g.119026708del	GRCh38
NC_000011.9:g.118897418del , CM000673.1:g.118897418del	GRCh37
NC_000011.8:g.118402628del	NCBI36
NG_013331.1:g.9198del , LRG_187:g.9198del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1014+229del
ENST00000697845.1:n.1167del
ENST00000697846.1:n.1014+229del
ENST00000697847.1:n.1015-20del
ENST00000697848.1:n.1015-20del
ENST00000697849.1:n.2282del
ENST00000697850.1:n.1015-20del
ENST00000697851.1:n.2603del
ENST00000638186.1:n.1089-20del
ENST00000638360.1:n.921-20del
ENST00000638925.1:n.1022-20del
ENST00000650539.1:n.1191-20del
ENST00000330775.9:c.785-20del	ENSP00000476242.2:n.785-20del
ENST00000357590.9:c.785-20del	ENSP00000476176.2:n.785-20del
ENST00000524428.5:n.1106+229del
ENST00000525039.5:n.1209-20del
ENST00000525102.5:n.1543-20del
ENST00000525372.5:n.786-20del
ENST00000526275.5:n.1567-20del
ENST00000527992.5:n.1013-20del
ENST00000529510.5:n.558+229del
ENST00000530407.5:n.935-20del
ENST00000532085.1:n.3624del
ENST00000532888.6:n.1309del
ENST00000538950.5:c.566-20del	ENSP00000475991.2:n.566-20del
ENST00000545985.5:c.785-20del	ENSP00000475241.2:n.785-20del
NM_001164277.1:c.785-20del , LRG_187t1:c.785-20del	NP_001157749.1:n.785-20del
NM_001164278.1:c.785-20del	NP_001157750.1:n.785-20del
NM_001164279.1:c.566-20del	NP_001157751.1:n.566-20del
NM_001164280.1:c.785-20del	NP_001157752.1:n.785-20del
NM_001467.5:c.785-20del	NP_001458.1:n.785-20del
NM_001164278.2:c.785-20del	NP_001157750.1:n.785-20del
NM_001164279.2:c.566-20del	NP_001157751.1:n.566-20del
NM_001164280.2:c.785-20del	NP_001157752.1:n.785-20del
NM_001467.6:c.785-20del	NP_001458.1:n.785-20del
NM_001164277.2:c.785-20del MANE Select	NP_001157749.1:n.785-20del