Canonical Allele Identifier: CA2616334671

Gene: SLC37A4

Linked Data

• gnomAD v4: 11-119026496-GCCAACC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026497_119026502del , CM000673.2:g.119026497_119026502del	GRCh38
NC_000011.9:g.118897207_118897212del , CM000673.1:g.118897207_118897212del	GRCh37
NC_000011.8:g.118402417_118402422del	NCBI36
NG_013331.1:g.9404_9409del , LRG_187:g.9404_9409del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1015-422_1015-417del
ENST00000697845.1:n.1373_1378del
ENST00000697846.1:n.1015-422_1015-417del
ENST00000697847.1:n.1201_1201+5del
ENST00000697848.1:n.1100+101_1100+106del
ENST00000697849.1:n.2488_2493del
ENST00000697850.1:n.1100+101_1100+106del
ENST00000697851.1:n.2708+101_2708+106del
ENST00000638186.1:n.1174+101_1174+106del
ENST00000638360.1:n.1006+101_1006+106del
ENST00000638925.1:n.1139+69_1139+74del
ENST00000650539.1:n.1276+101_1276+106del
ENST00000330775.9:c.870+101_870+106del	ENSP00000476242.2:n.870+101_870+106del
ENST00000357590.9:c.870+101_870+106del	ENSP00000476176.2:n.870+101_870+106del
ENST00000524428.5:n.1107-422_1107-417del
ENST00000525039.5:n.1294+101_1294+106del
ENST00000525102.5:n.1628+101_1628+106del
ENST00000525372.5:n.968+4_968+9del
ENST00000526275.5:n.1652+101_1652+106del
ENST00000527992.5:n.1098+101_1098+106del
ENST00000529510.5:n.559-422_559-417del
ENST00000530407.5:n.1020+101_1020+106del
ENST00000532085.1:n.3830_3835del
ENST00000538950.5:c.651+101_651+106del	ENSP00000475991.2:n.651+101_651+106del
ENST00000545985.5:c.870+101_870+106del	ENSP00000475241.2:n.870+101_870+106del
NM_001164277.1:c.870+101_870+106del , LRG_187t1:c.870+101_870+106del	NP_001157749.1:n.870+101_870+106del
NM_001164278.1:c.870+101_870+106del	NP_001157750.1:n.870+101_870+106del
NM_001164279.1:c.651+101_651+106del	NP_001157751.1:n.651+101_651+106del
NM_001164280.1:c.870+101_870+106del	NP_001157752.1:n.870+101_870+106del
NM_001467.5:c.870+101_870+106del	NP_001458.1:n.870+101_870+106del
NM_001164278.2:c.870+101_870+106del	NP_001157750.1:n.870+101_870+106del
NM_001164279.2:c.651+101_651+106del	NP_001157751.1:n.651+101_651+106del
NM_001164280.2:c.870+101_870+106del	NP_001157752.1:n.870+101_870+106del
NM_001467.6:c.870+101_870+106del	NP_001458.1:n.870+101_870+106del
NM_001164277.2:c.870+101_870+106del MANE Select	NP_001157749.1:n.870+101_870+106del