Canonical Allele Identifier: CA2003749539

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027431_119027433delinsGCA , CM000673.2:g.119027431_119027433delinsGCA	GRCh38
NC_000011.9:g.118898141_118898143delinsGCA , CM000673.1:g.118898141_118898143delinsGCA	GRCh37
NC_000011.8:g.118403351_118403353delinsGCA	NCBI36
NG_013331.1:g.8473_8475delinsTGC , LRG_187:g.8473_8475delinsTGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.855+195_855+197delinsTGC
ENST00000697845.1:n.779+195_779+197delinsTGC
ENST00000697846.1:n.855+195_855+197delinsTGC
ENST00000697847.1:n.855+195_855+197delinsTGC
ENST00000697848.1:n.855+195_855+197delinsTGC
ENST00000697849.1:n.1894+195_1894+197delinsTGC
ENST00000697850.1:n.855+195_855+197delinsTGC
ENST00000697851.1:n.2215+195_2215+197delinsTGC
ENST00000638186.1:n.929+195_929+197delinsTGC
ENST00000638360.1:n.761+195_761+197delinsTGC
ENST00000638925.1:n.862+195_862+197delinsTGC
ENST00000650539.1:n.1031+195_1031+197delinsTGC
ENST00000330775.9:c.625+195_625+197delinsTGC	ENSP00000476242.2:n.625+195_625+197delinsTGC
ENST00000357590.9:c.625+195_625+197delinsTGC	ENSP00000476176.2:n.625+195_625+197delinsTGC
ENST00000524428.5:n.947+195_947+197delinsTGC
ENST00000525039.5:n.1049+195_1049+197delinsTGC
ENST00000525102.5:n.1383+195_1383+197delinsTGC
ENST00000525372.5:n.626+195_626+197delinsTGC
ENST00000526275.5:n.1407+195_1407+197delinsTGC
ENST00000526626.6:n.588+195_588+197delinsTGC
ENST00000527992.5:n.853+195_853+197delinsTGC
ENST00000529510.5:n.400-338_400-336delinsTGC
ENST00000530407.5:n.775+195_775+197delinsTGC
ENST00000532085.1:n.3236+195_3236+197delinsTGC
ENST00000532888.6:n.921+195_921+197delinsTGC
ENST00000538950.5:c.406+195_406+197delinsTGC	ENSP00000475991.2:n.406+195_406+197delinsTGC
ENST00000545985.5:c.625+195_625+197delinsTGC	ENSP00000475241.2:n.625+195_625+197delinsTGC
NM_001164277.1:c.625+195_625+197delinsTGC , LRG_187t1:c.625+195_625+197delinsTGC	NP_001157749.1:n.625+195_625+197delinsTGC
NM_001164278.1:c.625+195_625+197delinsTGC	NP_001157750.1:n.625+195_625+197delinsTGC
NM_001164279.1:c.406+195_406+197delinsTGC	NP_001157751.1:n.406+195_406+197delinsTGC
NM_001164280.1:c.625+195_625+197delinsTGC	NP_001157752.1:n.625+195_625+197delinsTGC
NM_001467.5:c.625+195_625+197delinsTGC	NP_001458.1:n.625+195_625+197delinsTGC
NM_001164278.2:c.625+195_625+197delinsTGC	NP_001157750.1:n.625+195_625+197delinsTGC
NM_001164279.2:c.406+195_406+197delinsTGC	NP_001157751.1:n.406+195_406+197delinsTGC
NM_001164280.2:c.625+195_625+197delinsTGC	NP_001157752.1:n.625+195_625+197delinsTGC
NM_001467.6:c.625+195_625+197delinsTGC	NP_001458.1:n.625+195_625+197delinsTGC
NM_001164277.2:c.625+195_625+197delinsTGC MANE Select	NP_001157749.1:n.625+195_625+197delinsTGC