Canonical Allele Identifier: CA2616336281

Gene: SLC37A4

Linked Data

• gnomAD v4: 11-119028151-CATCCTCTATGACA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119028156_119028168del , CM000673.2:g.119028156_119028168del	GRCh38
NC_000011.9:g.118898866_118898878del , CM000673.1:g.118898866_118898878del	GRCh37
NC_000011.8:g.118404076_118404088del	NCBI36
NG_013331.1:g.7743_7755del , LRG_187:g.7743_7755del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.610+30_610+42del
ENST00000697845.1:n.534+30_534+42del
ENST00000697846.1:n.610+30_610+42del
ENST00000697847.1:n.610+30_610+42del
ENST00000697848.1:n.610+30_610+42del
ENST00000697849.1:n.1649+30_1649+42del
ENST00000697850.1:n.610+30_610+42del
ENST00000697851.1:n.1679_1691del
ENST00000638186.1:n.684+30_684+42del
ENST00000638360.1:n.618+30_618+42del
ENST00000638925.1:n.617+30_617+42del
ENST00000650539.1:n.786+30_786+42del
ENST00000330775.9:c.381+30_381+42del	ENSP00000476242.2:n.381+30_381+42del
ENST00000357590.9:c.381+30_381+42del	ENSP00000476176.2:n.381+30_381+42del
ENST00000524428.5:n.411_423del
ENST00000525039.5:n.804+30_804+42del
ENST00000525102.5:n.1138+30_1138+42del
ENST00000525372.5:n.381+30_381+42del
ENST00000525787.1:n.706_718del
ENST00000526275.5:n.871_883del
ENST00000526626.6:n.344-292_344-280del
ENST00000527992.5:n.608+30_608+42del
ENST00000529510.5:n.399+30_399+42del
ENST00000530407.5:n.530+30_530+42del
ENST00000532085.1:n.2700_2712del
ENST00000532888.6:n.676+30_676+42del
ENST00000538950.5:c.162+30_162+42del	ENSP00000475991.2:n.162+30_162+42del
ENST00000545985.5:c.381+30_381+42del	ENSP00000475241.2:n.381+30_381+42del
NM_001164277.1:c.381+30_381+42del , LRG_187t1:c.381+30_381+42del	NP_001157749.1:n.381+30_381+42del
NM_001164278.1:c.381+30_381+42del	NP_001157750.1:n.381+30_381+42del
NM_001164279.1:c.162+30_162+42del	NP_001157751.1:n.162+30_162+42del
NM_001164280.1:c.381+30_381+42del	NP_001157752.1:n.381+30_381+42del
NM_001467.5:c.381+30_381+42del	NP_001458.1:n.381+30_381+42del
NM_001164278.2:c.381+30_381+42del	NP_001157750.1:n.381+30_381+42del
NM_001164279.2:c.162+30_162+42del	NP_001157751.1:n.162+30_162+42del
NM_001164280.2:c.381+30_381+42del	NP_001157752.1:n.381+30_381+42del
NM_001467.6:c.381+30_381+42del	NP_001458.1:n.381+30_381+42del
NM_001164277.2:c.381+30_381+42del MANE Select	NP_001157749.1:n.381+30_381+42del