Canonical Allele Identifier: CA2575003446

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029433_119029440del , CM000673.2:g.119029433_119029440del	GRCh38
NC_000011.9:g.118900143_118900150del , CM000673.1:g.118900143_118900150del	GRCh37
NC_000011.8:g.118405353_118405360del	NCBI36
NG_013331.1:g.6468_6475del , LRG_187:g.6468_6475del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.160_167del
ENST00000697846.1:n.160_167del
ENST00000697847.1:n.160_167del
ENST00000697848.1:n.160_167del
ENST00000697849.1:n.404_411del
ENST00000697850.1:n.160_167del
ENST00000697851.1:n.404_411del
ENST00000638186.1:n.234_241del
ENST00000638360.1:n.168_175del
ENST00000638925.1:n.167_174del
ENST00000650539.1:n.336_343del
ENST00000330775.9:c.-70_-63del	ENSP00000476242.2:n.-70_-63del
ENST00000357590.9:c.-70_-63del	ENSP00000476176.2:n.-70_-63del
ENST00000525039.5:n.354_361del
ENST00000525102.5:n.688_695del
ENST00000525787.1:n.226_233del
ENST00000526626.6:n.126_133del
ENST00000527992.5:n.158_165del
ENST00000530407.5:n.150_157del
ENST00000532085.1:n.1425_1432del
ENST00000532888.6:n.126_133del
ENST00000534384.1:n.151_158del
ENST00000538950.5:c.-219_-212del	ENSP00000475991.2:n.-219_-212del
ENST00000545985.5:c.-70_-63del	ENSP00000475241.2:n.-70_-63del
NM_001164277.1:c.-70_-63del , LRG_187t1:c.-70_-63del	NP_001157749.1:n.-70_-63del
NM_001164278.1:c.-70_-63del	NP_001157750.1:n.-70_-63del
NM_001164279.1:c.-219_-212del	NP_001157751.1:n.-219_-212del
NM_001164280.1:c.-70_-63del	NP_001157752.1:n.-70_-63del
NM_001467.5:c.-70_-63del	NP_001458.1:n.-70_-63del
NM_001164278.2:c.-70_-63del	NP_001157750.1:n.-70_-63del
NM_001164279.2:c.-219_-212del	NP_001157751.1:n.-219_-212del
NM_001164280.2:c.-70_-63del	NP_001157752.1:n.-70_-63del
NM_001467.6:c.-70_-63del	NP_001458.1:n.-70_-63del
NM_001164277.2:c.-70_-63del MANE Select	NP_001157749.1:n.-70_-63del