Canonical Allele Identifier: CA2616341250

Gene: SLC37A4

Linked Data

• gnomAD v4: 11-119029948-TACC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029949_119029951del , CM000673.2:g.119029949_119029951del	GRCh38
NC_000011.9:g.118900659_118900661del , CM000673.1:g.118900659_118900661del	GRCh37
NC_000011.8:g.118405869_118405871del	NCBI36
NG_013331.1:g.5956_5958del , LRG_187:g.5956_5958del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.35-387_35-385del
ENST00000697846.1:n.35-387_35-385del
ENST00000697847.1:n.35-387_35-385del
ENST00000697848.1:n.35-387_35-385del
ENST00000697850.1:n.35-387_35-385del
ENST00000638186.1:n.24_26del
ENST00000638360.1:n.43-387_43-385del
ENST00000638925.1:n.42-387_42-385del
ENST00000650539.1:n.210+219_210+221del
ENST00000330775.9:c.-195-387_-195-385del	ENSP00000476242.2:n.-195-387_-195-385del
ENST00000357590.9:c.-195-387_-195-385del	ENSP00000476176.2:n.-195-387_-195-385del
ENST00000525039.5:n.229-387_229-385del
ENST00000525102.5:n.562+281_562+283del
ENST00000527992.5:n.33-387_33-385del
ENST00000530407.5:n.25-387_25-385del
ENST00000532085.1:n.913_915del
ENST00000538950.5:c.-344-387_-344-385del	ENSP00000475991.2:n.-344-387_-344-385del
ENST00000545985.5:c.-196+281_-196+283del	ENSP00000475241.2:n.-196+281_-196+283del
NM_001164277.1:c.-196+281_-196+283del , LRG_187t1:c.-196+281_-196+283del	NP_001157749.1:n.-196+281_-196+283del
NM_001164278.1:c.-195-387_-195-385del	NP_001157750.1:n.-195-387_-195-385del
NM_001164279.1:c.-344-387_-344-385del	NP_001157751.1:n.-344-387_-344-385del
NM_001467.5:c.-195-387_-195-385del	NP_001458.1:n.-195-387_-195-385del
NM_001164278.2:c.-195-387_-195-385del	NP_001157750.1:n.-195-387_-195-385del
NM_001164279.2:c.-344-387_-344-385del	NP_001157751.1:n.-344-387_-344-385del
NM_001467.6:c.-195-387_-195-385del	NP_001458.1:n.-195-387_-195-385del
NM_001164277.2:c.-196+281_-196+283del MANE Select	NP_001157749.1:n.-196+281_-196+283del