Canonical Allele Identifier: CA2616335759

Gene: SLC37A4

Linked Data

• dbSNP Id: rs2134637653
• gnomAD v4: 11-119027723-ACAC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027727_119027729del , CM000673.2:g.119027727_119027729del	GRCh38
NC_000011.9:g.118898437_118898439del , CM000673.1:g.118898437_118898439del	GRCh37
NC_000011.8:g.118403647_118403649del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.757_759del
ENST00000697845.1:n.681_683del
ENST00000697846.1:n.757_759del
ENST00000697847.1:n.757_759del
ENST00000697848.1:n.757_759del
ENST00000697849.1:n.1796_1798del
ENST00000697850.1:n.757_759del
ENST00000697851.1:n.2117_2119del
ENST00000638186.1:n.831_833del
ENST00000638360.1:n.663_665del
ENST00000638925.1:n.764_766del
ENST00000650539.1:n.933_935del
ENST00000330775.9:c.528_529del
ENST00000357590.9:c.528_529del
ENST00000524428.5:n.849_851del
ENST00000525039.5:n.951_953del
ENST00000525102.5:n.1285_1287del
ENST00000525372.5:n.528_530del
ENST00000526275.5:n.1309_1311del
ENST00000526626.6:n.490_492del
ENST00000527992.5:n.755_757del
ENST00000529510.5:n.399+468_399+470del
ENST00000530407.5:n.677_679del
ENST00000532085.1:n.3138_3140del
ENST00000532888.6:n.823_825del
ENST00000538950.5:c.309_310del
ENST00000545985.5:c.528_529del