Canonical Allele Identifier: CA2616340588

Gene: SLC37A4

Linked Data

• gnomAD v4: 11-119029113-C-CAA

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029113_119029114insAA , CM000673.2:g.119029113_119029114insAA	GRCh38
NC_000011.9:g.118899823_118899824insAA , CM000673.1:g.118899823_118899824insAA	GRCh37
NC_000011.8:g.118405033_118405034insAA	NCBI36
NG_013331.1:g.6793_6794insTT , LRG_187:g.6793_6794insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.377+108_377+109insTT
ENST00000697846.1:n.377+108_377+109insTT
ENST00000697847.1:n.377+108_377+109insTT
ENST00000697848.1:n.377+108_377+109insTT
ENST00000697849.1:n.729_730insTT
ENST00000697850.1:n.377+108_377+109insTT
ENST00000697851.1:n.729_730insTT
ENST00000638186.1:n.451+108_451+109insTT
ENST00000638360.1:n.385+108_385+109insTT
ENST00000638925.1:n.384+108_384+109insTT
ENST00000650539.1:n.553+108_553+109insTT
ENST00000330775.9:c.148+108_148+109insTT	ENSP00000476242.2:n.148+108_148+109insTT
ENST00000357590.9:c.148+108_148+109insTT	ENSP00000476176.2:n.148+108_148+109insTT
ENST00000524428.5:n.148+108_148+109insTT
ENST00000525039.5:n.571+108_571+109insTT
ENST00000525102.5:n.905+108_905+109insTT
ENST00000525372.5:n.148+108_148+109insTT
ENST00000525787.1:n.443+108_443+109insTT
ENST00000526626.6:n.343+108_343+109insTT
ENST00000527992.5:n.375+108_375+109insTT
ENST00000529510.5:n.166+108_166+109insTT
ENST00000530407.5:n.197+278_198-279insTT
ENST00000532085.1:n.1750_1751insTT
ENST00000532888.6:n.343+108_343+109insTT
ENST00000534384.1:n.368+108_368+109insTT
ENST00000538950.5:c.-172+278_-171-279insTT	ENSP00000475991.2:n.-172+278_-171-279insTT
ENST00000545985.5:c.148+108_148+109insTT	ENSP00000475241.2:n.148+108_148+109insTT
NM_001164277.1:c.148+108_148+109insTT , LRG_187t1:c.148+108_148+109insTT	NP_001157749.1:n.148+108_148+109insTT
NM_001164278.1:c.148+108_148+109insTT	NP_001157750.1:n.148+108_148+109insTT
NM_001164279.1:c.-172+278_-171-279insTT	NP_001157751.1:n.-172+278_-171-279insTT
NM_001164280.1:c.148+108_148+109insTT	NP_001157752.1:n.148+108_148+109insTT
NM_001467.5:c.148+108_148+109insTT	NP_001458.1:n.148+108_148+109insTT
NM_001164278.2:c.148+108_148+109insTT	NP_001157750.1:n.148+108_148+109insTT
NM_001164279.2:c.-172+278_-171-279insTT	NP_001157751.1:n.-172+278_-171-279insTT
NM_001164280.2:c.148+108_148+109insTT	NP_001157752.1:n.148+108_148+109insTT
NM_001467.6:c.148+108_148+109insTT	NP_001458.1:n.148+108_148+109insTT
NM_001164277.2:c.148+108_148+109insTT MANE Select	NP_001157749.1:n.148+108_148+109insTT