Canonical Allele Identifier: CA2003749181

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026714_119026719delinsGAGGGA , CM000673.2:g.119026714_119026719delinsGAGGGA	GRCh38
NC_000011.9:g.118897424_118897429delinsGAGGGA , CM000673.1:g.118897424_118897429delinsGAGGGA	GRCh37
NC_000011.8:g.118402634_118402639delinsGAGGGA	NCBI36
NG_013331.1:g.9187_9192delinsTCCCTC , LRG_187:g.9187_9192delinsTCCCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1014+218_1014+223delinsTCCCTC
ENST00000697845.1:n.1156_1161delinsTCCCTC
ENST00000697846.1:n.1014+218_1014+223delinsTCCCTC
ENST00000697847.1:n.1015-31_1015-26delinsTCCCTC
ENST00000697848.1:n.1015-31_1015-26delinsTCCCTC
ENST00000697849.1:n.2271_2276delinsTCCCTC
ENST00000697850.1:n.1015-31_1015-26delinsTCCCTC
ENST00000697851.1:n.2592_2597delinsTCCCTC
ENST00000638186.1:n.1089-31_1089-26delinsTCCCTC
ENST00000638360.1:n.921-31_921-26delinsTCCCTC
ENST00000638925.1:n.1022-31_1022-26delinsTCCCTC
ENST00000650539.1:n.1191-31_1191-26delinsTCCCTC
ENST00000330775.9:c.785-31_785-26delinsTCCCTC	ENSP00000476242.2:n.785-31_785-26delinsTCCCTC
ENST00000357590.9:c.785-31_785-26delinsTCCCTC	ENSP00000476176.2:n.785-31_785-26delinsTCCCTC
ENST00000524428.5:n.1106+218_1106+223delinsTCCCTC
ENST00000525039.5:n.1209-31_1209-26delinsTCCCTC
ENST00000525102.5:n.1543-31_1543-26delinsTCCCTC
ENST00000525372.5:n.786-31_786-26delinsTCCCTC
ENST00000526275.5:n.1567-31_1567-26delinsTCCCTC
ENST00000527992.5:n.1013-31_1013-26delinsTCCCTC
ENST00000529510.5:n.558+218_558+223delinsTCCCTC
ENST00000530407.5:n.935-31_935-26delinsTCCCTC
ENST00000532085.1:n.3613_3618delinsTCCCTC
ENST00000532888.6:n.1298_1303delinsTCCCTC
ENST00000538950.5:c.566-31_566-26delinsTCCCTC	ENSP00000475991.2:n.566-31_566-26delinsTCCCTC
ENST00000545985.5:c.785-31_785-26delinsTCCCTC	ENSP00000475241.2:n.785-31_785-26delinsTCCCTC
NM_001164277.1:c.785-31_785-26delinsTCCCTC , LRG_187t1:c.785-31_785-26delinsTCCCTC	NP_001157749.1:n.785-31_785-26delinsTCCCTC
NM_001164278.1:c.785-31_785-26delinsTCCCTC	NP_001157750.1:n.785-31_785-26delinsTCCCTC
NM_001164279.1:c.566-31_566-26delinsTCCCTC	NP_001157751.1:n.566-31_566-26delinsTCCCTC
NM_001164280.1:c.785-31_785-26delinsTCCCTC	NP_001157752.1:n.785-31_785-26delinsTCCCTC
NM_001467.5:c.785-31_785-26delinsTCCCTC	NP_001458.1:n.785-31_785-26delinsTCCCTC
NM_001164278.2:c.785-31_785-26delinsTCCCTC	NP_001157750.1:n.785-31_785-26delinsTCCCTC
NM_001164279.2:c.566-31_566-26delinsTCCCTC	NP_001157751.1:n.566-31_566-26delinsTCCCTC
NM_001164280.2:c.785-31_785-26delinsTCCCTC	NP_001157752.1:n.785-31_785-26delinsTCCCTC
NM_001467.6:c.785-31_785-26delinsTCCCTC	NP_001458.1:n.785-31_785-26delinsTCCCTC
NM_001164277.2:c.785-31_785-26delinsTCCCTC MANE Select	NP_001157749.1:n.785-31_785-26delinsTCCCTC