Canonical Allele Identifier: CA2616340287

Gene: SLC37A4

Linked Data

• gnomAD v4: 11-119028840-G-GTACC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119028840_119028841insTACC , CM000673.2:g.119028840_119028841insTACC	GRCh38
NC_000011.9:g.118899550_118899551insTACC , CM000673.1:g.118899550_118899551insTACC	GRCh37
NC_000011.8:g.118404760_118404761insTACC	NCBI36
NG_013331.1:g.7066_7067insGGTA , LRG_187:g.7066_7067insGGTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.377+381_377+382insGGTA
ENST00000697846.1:n.377+381_377+382insGGTA
ENST00000697847.1:n.377+381_377+382insGGTA
ENST00000697848.1:n.377+381_377+382insGGTA
ENST00000697849.1:n.1002_1003insGGTA
ENST00000697850.1:n.377+381_377+382insGGTA
ENST00000697851.1:n.1002_1003insGGTA
ENST00000638186.1:n.451+381_451+382insGGTA
ENST00000638360.1:n.385+381_385+382insGGTA
ENST00000638925.1:n.384+381_384+382insGGTA
ENST00000650539.1:n.553+381_553+382insGGTA
ENST00000330775.9:c.148+381_148+382insGGTA	ENSP00000476242.2:n.148+381_148+382insGGTA
ENST00000357590.9:c.148+381_148+382insGGTA	ENSP00000476176.2:n.148+381_148+382insGGTA
ENST00000524428.5:n.148+381_148+382insGGTA
ENST00000525039.5:n.571+381_571+382insGGTA
ENST00000525102.5:n.905+381_905+382insGGTA
ENST00000525372.5:n.148+381_148+382insGGTA
ENST00000525787.1:n.443+381_443+382insGGTA
ENST00000526275.5:n.194_195insGGTA
ENST00000526626.6:n.343+381_343+382insGGTA
ENST00000527992.5:n.375+381_375+382insGGTA
ENST00000529510.5:n.166+381_166+382insGGTA
ENST00000530407.5:n.198-7_198-6insGGTA
ENST00000532085.1:n.2023_2024insGGTA
ENST00000532888.6:n.344-7_344-6insGGTA
ENST00000534384.1:n.368+381_368+382insGGTA
ENST00000538950.5:c.-171-7_-171-6insGGTA	ENSP00000475991.2:n.-171-7_-171-6insGGTA
ENST00000545985.5:c.148+381_148+382insGGTA	ENSP00000475241.2:n.148+381_148+382insGGTA
NM_001164277.1:c.148+381_148+382insGGTA , LRG_187t1:c.148+381_148+382insGGTA	NP_001157749.1:n.148+381_148+382insGGTA
NM_001164278.1:c.148+381_148+382insGGTA	NP_001157750.1:n.148+381_148+382insGGTA
NM_001164279.1:c.-171-7_-171-6insGGTA	NP_001157751.1:n.-171-7_-171-6insGGTA
NM_001164280.1:c.148+381_148+382insGGTA	NP_001157752.1:n.148+381_148+382insGGTA
NM_001467.5:c.148+381_148+382insGGTA	NP_001458.1:n.148+381_148+382insGGTA
NM_001164278.2:c.148+381_148+382insGGTA	NP_001157750.1:n.148+381_148+382insGGTA
NM_001164279.2:c.-171-7_-171-6insGGTA	NP_001157751.1:n.-171-7_-171-6insGGTA
NM_001164280.2:c.148+381_148+382insGGTA	NP_001157752.1:n.148+381_148+382insGGTA
NM_001467.6:c.148+381_148+382insGGTA	NP_001458.1:n.148+381_148+382insGGTA
NM_001164277.2:c.148+381_148+382insGGTA MANE Select	NP_001157749.1:n.148+381_148+382insGGTA