Canonical Allele Identifier: CA2616341258

Gene: SLC37A4

Linked Data

• gnomAD v4: 11-119029960-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029960_119029961insA , CM000673.2:g.119029960_119029961insA	GRCh38
NC_000011.9:g.118900670_118900671insA , CM000673.1:g.118900670_118900671insA	GRCh37
NC_000011.8:g.118405880_118405881insA	NCBI36
NG_013331.1:g.5946_5947insT , LRG_187:g.5946_5947insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.35-397_35-396insT
ENST00000697846.1:n.35-397_35-396insT
ENST00000697847.1:n.35-397_35-396insT
ENST00000697848.1:n.35-397_35-396insT
ENST00000697850.1:n.35-397_35-396insT
ENST00000638186.1:n.14_15insT
ENST00000638360.1:n.43-397_43-396insT
ENST00000638925.1:n.42-397_42-396insT
ENST00000650539.1:n.210+209_210+210insT
ENST00000330775.9:c.-195-397_-195-396insT	ENSP00000476242.2:n.-195-397_-195-396insT
ENST00000357590.9:c.-195-397_-195-396insT	ENSP00000476176.2:n.-195-397_-195-396insT
ENST00000525039.5:n.229-397_229-396insT
ENST00000525102.5:n.562+271_562+272insT
ENST00000527992.5:n.33-397_33-396insT
ENST00000530407.5:n.25-397_25-396insT
ENST00000532085.1:n.903_904insT
ENST00000538950.5:c.-344-397_-344-396insT	ENSP00000475991.2:n.-344-397_-344-396insT
ENST00000545985.5:c.-196+271_-196+272insT	ENSP00000475241.2:n.-196+271_-196+272insT
NM_001164277.1:c.-196+271_-196+272insT , LRG_187t1:c.-196+271_-196+272insT	NP_001157749.1:n.-196+271_-196+272insT
NM_001164278.1:c.-195-397_-195-396insT	NP_001157750.1:n.-195-397_-195-396insT
NM_001164279.1:c.-344-397_-344-396insT	NP_001157751.1:n.-344-397_-344-396insT
NM_001467.5:c.-195-397_-195-396insT	NP_001458.1:n.-195-397_-195-396insT
NM_001164278.2:c.-195-397_-195-396insT	NP_001157750.1:n.-195-397_-195-396insT
NM_001164279.2:c.-344-397_-344-396insT	NP_001157751.1:n.-344-397_-344-396insT
NM_001467.6:c.-195-397_-195-396insT	NP_001458.1:n.-195-397_-195-396insT
NM_001164277.2:c.-196+271_-196+272insT MANE Select	NP_001157749.1:n.-196+271_-196+272insT