Canonical Allele Identifier: CA2616339988

Gene: SLC37A4

Linked Data

• ClinVar Variation Id: 2697074
• ClinVar RCV Id: RCV003507617
• gnomAD v4: 11-119026070-GACAGTCCCGCCTATGGAT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026080_119026097del , CM000673.2:g.119026080_119026097del	GRCh38
NC_000011.9:g.118896790_118896807del , CM000673.1:g.118896790_118896807del	GRCh37
NC_000011.8:g.118402000_118402017del	NCBI36
NG_013331.1:g.9818_9835del , LRG_187:g.9818_9835del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1015-8_1024del
ENST00000697845.1:n.1787_1804del
ENST00000697846.1:n.1015-8_1024del
ENST00000697847.1:n.1202-331_1202-314del
ENST00000697848.1:n.1101-8_1110del
ENST00000697849.1:n.2902_2919del
ENST00000697850.1:n.1101-8_1110del
ENST00000697851.1:n.2709-8_2718del
ENST00000638186.1:n.1175-8_1184del
ENST00000638360.1:n.1007-8_1016del
ENST00000638925.1:n.1140-8_1149del
ENST00000650539.1:n.1277-8_1286del
ENST00000330775.9:c.871-8_880del
ENST00000357590.9:c.871-8_880del
ENST00000524428.5:n.1107-8_1116del
ENST00000525039.5:n.1295-8_1304del
ENST00000525102.5:n.1629-8_1638del
ENST00000525372.5:n.969-8_978del
ENST00000526275.5:n.1653-8_1662del
ENST00000527992.5:n.1099-8_1108del
ENST00000529510.5:n.559-8_568del
ENST00000530407.5:n.1021-8_1030del
ENST00000532085.1:n.4244_4261del
ENST00000538950.5:c.652-8_661del
ENST00000545985.5:c.871-8_880del
NM_001164277.1:c.871-8_880del , LRG_187t1:c.871-8_880del
NM_001164278.1:c.871-8_880del
NM_001164279.1:c.652-8_661del
NM_001164280.1:c.871-8_880del
NM_001467.5:c.871-8_880del
NM_001164278.2:c.871-8_880del
NM_001164279.2:c.652-8_661del
NM_001164280.2:c.871-8_880del
NM_001467.6:c.871-8_880del
NM_001164277.2:c.871-8_880del