Canonical Allele Identifier: CA2575003312

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026909_119026918del , CM000673.2:g.119026909_119026918del	GRCh38
NC_000011.9:g.118897619_118897628del , CM000673.1:g.118897619_118897628del	GRCh37
NC_000011.8:g.118402829_118402838del	NCBI36
NG_013331.1:g.8990_8999del , LRG_187:g.8990_8999del

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.1014+21_1014+30del
ENST00000697845.1:n.959_968del
ENST00000697846.1:n.1014+21_1014+30del
ENST00000697847.1:n.1014+21_1014+30del
ENST00000697848.1:n.1014+21_1014+30del
ENST00000697849.1:n.2074_2083del
ENST00000697850.1:n.1014+21_1014+30del
ENST00000697851.1:n.2395_2404del
ENST00000638186.1:n.1088+21_1088+30del
ENST00000638360.1:n.920+21_920+30del
ENST00000638925.1:n.1021+21_1021+30del
ENST00000650539.1:n.1190+21_1190+30del
ENST00000330775.9:c.784+21_784+30del	ENSP00000476242.2:n.784+21_784+30del
ENST00000357590.9:c.784+21_784+30del	ENSP00000476176.2:n.784+21_784+30del
ENST00000524428.5:n.1106+21_1106+30del
ENST00000525039.5:n.1208+21_1208+30del
ENST00000525102.5:n.1542+21_1542+30del
ENST00000525372.5:n.785+21_785+30del
ENST00000526275.5:n.1566+21_1566+30del
ENST00000527992.5:n.1012+21_1012+30del
ENST00000529510.5:n.558+21_558+30del
ENST00000530407.5:n.934+21_934+30del
ENST00000532085.1:n.3416_3425del
ENST00000532888.6:n.1101_1110del
ENST00000538950.5:c.565+21_565+30del	ENSP00000475991.2:n.565+21_565+30del
ENST00000545985.5:c.784+21_784+30del	ENSP00000475241.2:n.784+21_784+30del
NM_001164277.1:c.784+21_784+30del , LRG_187t1:c.784+21_784+30del	NP_001157749.1:n.784+21_784+30del
NM_001164278.1:c.784+21_784+30del	NP_001157750.1:n.784+21_784+30del
NM_001164279.1:c.565+21_565+30del	NP_001157751.1:n.565+21_565+30del
NM_001164280.1:c.784+21_784+30del	NP_001157752.1:n.784+21_784+30del
NM_001467.5:c.784+21_784+30del	NP_001458.1:n.784+21_784+30del
NM_001164278.2:c.784+21_784+30del	NP_001157750.1:n.784+21_784+30del
NM_001164279.2:c.565+21_565+30del	NP_001157751.1:n.565+21_565+30del
NM_001164280.2:c.784+21_784+30del	NP_001157752.1:n.784+21_784+30del
NM_001467.6:c.784+21_784+30del	NP_001458.1:n.784+21_784+30del
NM_001164277.2:c.784+21_784+30del MANE Select	NP_001157749.1:n.784+21_784+30del