Canonical Allele Identifier: CA2975979260

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026542_119026543del , CM000673.2:g.119026542_119026543del	GRCh38
NC_000011.9:g.118897252_118897253del , CM000673.1:g.118897252_118897253del	GRCh37
NC_000011.8:g.118402462_118402463del	NCBI36
NG_013331.1:g.9364_9365del , LRG_187:g.9364_9365del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1014+395_1014+396del
ENST00000697845.1:n.1333_1334del
ENST00000697846.1:n.1014+395_1014+396del
ENST00000697847.1:n.1161_1162del
ENST00000697848.1:n.1100+61_1100+62del
ENST00000697849.1:n.2448_2449del
ENST00000697850.1:n.1100+61_1100+62del
ENST00000697851.1:n.2708+61_2708+62del
ENST00000638186.1:n.1174+61_1174+62del
ENST00000638360.1:n.1006+61_1006+62del
ENST00000638925.1:n.1139+29_1139+30del
ENST00000650539.1:n.1276+61_1276+62del
ENST00000330775.9:c.870+61_870+62del	ENSP00000476242.2:n.870+61_870+62del
ENST00000357590.9:c.870+61_870+62del	ENSP00000476176.2:n.870+61_870+62del
ENST00000524428.5:n.1106+395_1106+396del
ENST00000525039.5:n.1294+61_1294+62del
ENST00000525102.5:n.1628+61_1628+62del
ENST00000525372.5:n.932_933del
ENST00000526275.5:n.1652+61_1652+62del
ENST00000527992.5:n.1098+61_1098+62del
ENST00000529510.5:n.558+395_558+396del
ENST00000530407.5:n.1020+61_1020+62del
ENST00000532085.1:n.3790_3791del
ENST00000538950.5:c.651+61_651+62del	ENSP00000475991.2:n.651+61_651+62del
ENST00000545985.5:c.870+61_870+62del	ENSP00000475241.2:n.870+61_870+62del
NM_001164277.1:c.870+61_870+62del , LRG_187t1:c.870+61_870+62del	NP_001157749.1:n.870+61_870+62del
NM_001164278.1:c.870+61_870+62del	NP_001157750.1:n.870+61_870+62del
NM_001164279.1:c.651+61_651+62del	NP_001157751.1:n.651+61_651+62del
NM_001164280.1:c.870+61_870+62del	NP_001157752.1:n.870+61_870+62del
NM_001467.5:c.870+61_870+62del	NP_001458.1:n.870+61_870+62del
NM_001164278.2:c.870+61_870+62del	NP_001157750.1:n.870+61_870+62del
NM_001164279.2:c.651+61_651+62del	NP_001157751.1:n.651+61_651+62del
NM_001164280.2:c.870+61_870+62del	NP_001157752.1:n.870+61_870+62del
NM_001467.6:c.870+61_870+62del	NP_001458.1:n.870+61_870+62del
NM_001164277.2:c.870+61_870+62del MANE Select	NP_001157749.1:n.870+61_870+62del