Canonical Allele Identifier: CA2616340313

Gene: SLC37A4

Linked Data

• gnomAD v4: 11-119028854-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119028856del , CM000673.2:g.119028856del	GRCh38
NC_000011.9:g.118899566del , CM000673.1:g.118899566del	GRCh37
NC_000011.8:g.118404776del	NCBI36
NG_013331.1:g.7052del , LRG_187:g.7052del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.377+367del
ENST00000697846.1:n.377+367del
ENST00000697847.1:n.377+367del
ENST00000697848.1:n.377+367del
ENST00000697849.1:n.988del
ENST00000697850.1:n.377+367del
ENST00000697851.1:n.988del
ENST00000638186.1:n.451+367del
ENST00000638360.1:n.385+367del
ENST00000638925.1:n.384+367del
ENST00000650539.1:n.553+367del
ENST00000330775.9:c.148+367del	ENSP00000476242.2:n.148+367del
ENST00000357590.9:c.148+367del	ENSP00000476176.2:n.148+367del
ENST00000524428.5:n.148+367del
ENST00000525039.5:n.571+367del
ENST00000525102.5:n.905+367del
ENST00000525372.5:n.148+367del
ENST00000525787.1:n.443+367del
ENST00000526275.5:n.180del
ENST00000526626.6:n.343+367del
ENST00000527992.5:n.375+367del
ENST00000529510.5:n.166+367del
ENST00000530407.5:n.198-21del
ENST00000532085.1:n.2009del
ENST00000532888.6:n.344-21del
ENST00000534384.1:n.368+367del
ENST00000538950.5:c.-171-21del	ENSP00000475991.2:n.-171-21del
ENST00000545985.5:c.148+367del	ENSP00000475241.2:n.148+367del
NM_001164277.1:c.148+367del , LRG_187t1:c.148+367del	NP_001157749.1:n.148+367del
NM_001164278.1:c.148+367del	NP_001157750.1:n.148+367del
NM_001164279.1:c.-171-21del	NP_001157751.1:n.-171-21del
NM_001164280.1:c.148+367del	NP_001157752.1:n.148+367del
NM_001467.5:c.148+367del	NP_001458.1:n.148+367del
NM_001164278.2:c.148+367del	NP_001157750.1:n.148+367del
NM_001164279.2:c.-171-21del	NP_001157751.1:n.-171-21del
NM_001164280.2:c.148+367del	NP_001157752.1:n.148+367del
NM_001467.6:c.148+367del	NP_001458.1:n.148+367del
NM_001164277.2:c.148+367del MANE Select	NP_001157749.1:n.148+367del