Canonical Allele Identifier: CA602577767

Gene: SLC37A4

Linked Data

• dbSNP Id: rs1565688944
• gnomAD v2: 11-118898132-CGA-C
• gnomAD v3: 11-119027422-CGA-C
• gnomAD v4: 11-119027422-CGA-C
• MyVariant Identifiers: chr11:g.118898133_118898134del (hg19) ; chr11:g.119027423_119027424del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027424_119027425del , CM000673.2:g.119027424_119027425del	GRCh38
NC_000011.9:g.118898134_118898135del , CM000673.1:g.118898134_118898135del	GRCh37
NC_000011.8:g.118403344_118403345del	NCBI36
NG_013331.1:g.8482_8483del , LRG_187:g.8482_8483del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.855+204_855+205del
ENST00000697845.1:n.779+204_779+205del
ENST00000697846.1:n.855+204_855+205del
ENST00000697847.1:n.855+204_855+205del
ENST00000697848.1:n.855+204_855+205del
ENST00000697849.1:n.1894+204_1894+205del
ENST00000697850.1:n.855+204_855+205del
ENST00000697851.1:n.2215+204_2215+205del
ENST00000638186.1:n.929+204_929+205del
ENST00000638360.1:n.761+204_761+205del
ENST00000638925.1:n.862+204_862+205del
ENST00000650539.1:n.1031+204_1031+205del
ENST00000330775.9:c.625+204_625+205del	ENSP00000476242.2:n.625+204_625+205del
ENST00000357590.9:c.625+204_625+205del	ENSP00000476176.2:n.625+204_625+205del
ENST00000524428.5:n.947+204_947+205del
ENST00000525039.5:n.1049+204_1049+205del
ENST00000525102.5:n.1383+204_1383+205del
ENST00000525372.5:n.626+204_626+205del
ENST00000526275.5:n.1407+204_1407+205del
ENST00000526626.6:n.588+204_588+205del
ENST00000527992.5:n.853+204_853+205del
ENST00000529510.5:n.400-329_400-328del
ENST00000530407.5:n.775+204_775+205del
ENST00000532085.1:n.3236+204_3236+205del
ENST00000532888.6:n.921+204_921+205del
ENST00000538950.5:c.406+204_406+205del	ENSP00000475991.2:n.406+204_406+205del
ENST00000545985.5:c.625+204_625+205del	ENSP00000475241.2:n.625+204_625+205del
NM_001164277.1:c.625+204_625+205del , LRG_187t1:c.625+204_625+205del	NP_001157749.1:n.625+204_625+205del
NM_001164278.1:c.625+204_625+205del	NP_001157750.1:n.625+204_625+205del
NM_001164279.1:c.406+204_406+205del	NP_001157751.1:n.406+204_406+205del
NM_001164280.1:c.625+204_625+205del	NP_001157752.1:n.625+204_625+205del
NM_001467.5:c.625+204_625+205del	NP_001458.1:n.625+204_625+205del
NM_001164278.2:c.625+204_625+205del	NP_001157750.1:n.625+204_625+205del
NM_001164279.2:c.406+204_406+205del	NP_001157751.1:n.406+204_406+205del
NM_001164280.2:c.625+204_625+205del	NP_001157752.1:n.625+204_625+205del
NM_001467.6:c.625+204_625+205del	NP_001458.1:n.625+204_625+205del
NM_001164277.2:c.625+204_625+205del MANE Select	NP_001157749.1:n.625+204_625+205del