Canonical Allele Identifier: CA912970985

Gene: SLC37A4

Linked Data

• MyVariant Identifiers: chr11:g.118897377_118897378del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026667_119026668del , CM000673.2:g.119026667_119026668del	GRCh38
NC_000011.9:g.118897377_118897378del , CM000673.1:g.118897377_118897378del	GRCh37
NC_000011.8:g.118402587_118402588del	NCBI36
NG_013331.1:g.9238_9239del , LRG_187:g.9238_9239del

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.1014+269_1014+270del
ENST00000697845.1:n.1207_1208del
ENST00000697846.1:n.1014+269_1014+270del
ENST00000697847.1:n.1035_1036del
ENST00000697848.1:n.1035_1036del
ENST00000697849.1:n.2322_2323del
ENST00000697850.1:n.1035_1036del
ENST00000697851.1:n.2643_2644del
ENST00000638186.1:n.1109_1110del
ENST00000638360.1:n.941_942del
ENST00000638925.1:n.1042_1043del
ENST00000650539.1:n.1211_1212del
ENST00000330775.9:c.805_806del	ENSP00000476242.2:p.Leu269GlyfsTer?
ENST00000357590.9:c.805_806del	ENSP00000476176.2:p.Leu269GlyfsTer?
ENST00000524428.5:n.1106+269_1106+270del
ENST00000525039.5:n.1229_1230del
ENST00000525102.5:n.1563_1564del
ENST00000525372.5:n.806_807del
ENST00000526275.5:n.1587_1588del
ENST00000527992.5:n.1033_1034del
ENST00000529510.5:n.558+269_558+270del
ENST00000530407.5:n.955_956del
ENST00000532085.1:n.3664_3665del
ENST00000532888.6:n.1349_1350del
ENST00000538950.5:c.586_587del	ENSP00000475991.2:p.Leu196GlyfsTer?
ENST00000545985.5:c.805_806del	ENSP00000475241.2:p.Leu269GlyfsTer?
NM_001164277.1:c.805_806del , LRG_187t1:c.805_806del	NP_001157749.1:p.Leu269GlyfsTer?
NM_001164278.1:c.805_806del	NP_001157750.1:p.Leu269GlyfsTer?
NM_001164279.1:c.586_587del	NP_001157751.1:p.Leu196GlyfsTer?
NM_001164280.1:c.805_806del	NP_001157752.1:p.Leu269GlyfsTer?
NM_001467.5:c.805_806del	NP_001458.1:p.Leu269GlyfsTer?
NM_001164278.2:c.805_806del	NP_001157750.1:p.Leu269GlyfsTer?
NM_001164279.2:c.586_587del	NP_001157751.1:p.Leu196GlyfsTer?
NM_001164280.2:c.805_806del	NP_001157752.1:p.Leu269GlyfsTer?
NM_001467.6:c.805_806del	NP_001458.1:p.Leu269GlyfsTer?
NM_001164277.2:c.805_806del MANE Select	NP_001157749.1:p.Leu269GlyfsTer?