Canonical Allele Identifier: CA2003749229

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026796_119026797delinsAG , CM000673.2:g.119026796_119026797delinsAG	GRCh38
NC_000011.9:g.118897506_118897507delinsAG , CM000673.1:g.118897506_118897507delinsAG	GRCh37
NC_000011.8:g.118402716_118402717delinsAG	NCBI36
NG_013331.1:g.9109_9110delinsCT , LRG_187:g.9109_9110delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1014+140_1014+141delinsCT
ENST00000697845.1:n.1078_1079delinsCT
ENST00000697846.1:n.1014+140_1014+141delinsCT
ENST00000697847.1:n.1015-109_1015-108delinsCT
ENST00000697848.1:n.1015-109_1015-108delinsCT
ENST00000697849.1:n.2193_2194delinsCT
ENST00000697850.1:n.1015-109_1015-108delinsCT
ENST00000697851.1:n.2514_2515delinsCT
ENST00000638186.1:n.1089-109_1089-108delinsCT
ENST00000638360.1:n.921-109_921-108delinsCT
ENST00000638925.1:n.1022-109_1022-108delinsCT
ENST00000650539.1:n.1191-109_1191-108delinsCT
ENST00000330775.9:c.785-109_785-108delinsCT	ENSP00000476242.2:n.785-109_785-108delinsCT
ENST00000357590.9:c.785-109_785-108delinsCT	ENSP00000476176.2:n.785-109_785-108delinsCT
ENST00000524428.5:n.1106+140_1106+141delinsCT
ENST00000525039.5:n.1209-109_1209-108delinsCT
ENST00000525102.5:n.1543-109_1543-108delinsCT
ENST00000525372.5:n.786-109_786-108delinsCT
ENST00000526275.5:n.1567-109_1567-108delinsCT
ENST00000527992.5:n.1013-109_1013-108delinsCT
ENST00000529510.5:n.558+140_558+141delinsCT
ENST00000530407.5:n.935-109_935-108delinsCT
ENST00000532085.1:n.3535_3536delinsCT
ENST00000532888.6:n.1220_1221delinsCT
ENST00000538950.5:c.566-109_566-108delinsCT	ENSP00000475991.2:n.566-109_566-108delinsCT
ENST00000545985.5:c.785-109_785-108delinsCT	ENSP00000475241.2:n.785-109_785-108delinsCT
NM_001164277.1:c.785-109_785-108delinsCT , LRG_187t1:c.785-109_785-108delinsCT	NP_001157749.1:n.785-109_785-108delinsCT
NM_001164278.1:c.785-109_785-108delinsCT	NP_001157750.1:n.785-109_785-108delinsCT
NM_001164279.1:c.566-109_566-108delinsCT	NP_001157751.1:n.566-109_566-108delinsCT
NM_001164280.1:c.785-109_785-108delinsCT	NP_001157752.1:n.785-109_785-108delinsCT
NM_001467.5:c.785-109_785-108delinsCT	NP_001458.1:n.785-109_785-108delinsCT
NM_001164278.2:c.785-109_785-108delinsCT	NP_001157750.1:n.785-109_785-108delinsCT
NM_001164279.2:c.566-109_566-108delinsCT	NP_001157751.1:n.566-109_566-108delinsCT
NM_001164280.2:c.785-109_785-108delinsCT	NP_001157752.1:n.785-109_785-108delinsCT
NM_001467.6:c.785-109_785-108delinsCT	NP_001458.1:n.785-109_785-108delinsCT
NM_001164277.2:c.785-109_785-108delinsCT MANE Select	NP_001157749.1:n.785-109_785-108delinsCT