Canonical Allele Identifier: CA2616340656

Gene: SLC37A4

Linked Data

• gnomAD v4: 11-119029359-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029362del , CM000673.2:g.119029362del	GRCh38
NC_000011.9:g.118900072del , CM000673.1:g.118900072del	GRCh37
NC_000011.8:g.118405282del	NCBI36
NG_013331.1:g.6547del , LRG_187:g.6547del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.239del
ENST00000697846.1:n.239del
ENST00000697847.1:n.239del
ENST00000697848.1:n.239del
ENST00000697849.1:n.483del
ENST00000697850.1:n.239del
ENST00000697851.1:n.483del
ENST00000638186.1:n.313del
ENST00000638360.1:n.247del
ENST00000638925.1:n.246del
ENST00000650539.1:n.415del
ENST00000330775.9:c.10del	ENSP00000476242.2:p.Gln4ArgfsTer9
ENST00000357590.9:c.10del	ENSP00000476176.2:p.Gln4ArgfsTer9
ENST00000524428.5:n.10del
ENST00000525039.5:n.433del
ENST00000525102.5:n.767del
ENST00000525372.5:n.10del
ENST00000525787.1:n.305del
ENST00000526626.6:n.205del
ENST00000527992.5:n.237del
ENST00000529510.5:n.28del
ENST00000530407.5:n.197+32del
ENST00000532085.1:n.1504del
ENST00000532888.6:n.205del
ENST00000534384.1:n.230del
ENST00000538950.5:c.-172+32del	ENSP00000475991.2:n.-172+32del
ENST00000545985.5:c.10del	ENSP00000475241.2:p.Gln4ArgfsTer9
NM_001164277.1:c.10del , LRG_187t1:c.10del	NP_001157749.1:p.Gln4ArgfsTer9
NM_001164278.1:c.10del	NP_001157750.1:p.Gln4ArgfsTer9
NM_001164279.1:c.-172+32del	NP_001157751.1:n.-172+32del
NM_001164280.1:c.10del	NP_001157752.1:p.Gln4ArgfsTer9
NM_001467.5:c.10del	NP_001458.1:p.Gln4ArgfsTer9
NM_001164278.2:c.10del	NP_001157750.1:p.Gln4ArgfsTer9
NM_001164279.2:c.-172+32del	NP_001157751.1:n.-172+32del
NM_001164280.2:c.10del	NP_001157752.1:p.Gln4ArgfsTer9
NM_001467.6:c.10del	NP_001458.1:p.Gln4ArgfsTer9
NM_001164277.2:c.10del MANE Select	NP_001157749.1:p.Gln4ArgfsTer9