Canonical Allele Identifier: CA2975984977

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029382del , CM000673.2:g.119029382del	GRCh38
NC_000011.9:g.118900092del , CM000673.1:g.118900092del	GRCh37
NC_000011.8:g.118405302del	NCBI36
NG_013331.1:g.6525del , LRG_187:g.6525del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.217del
ENST00000697846.1:n.217del
ENST00000697847.1:n.217del
ENST00000697848.1:n.217del
ENST00000697849.1:n.461del
ENST00000697850.1:n.217del
ENST00000697851.1:n.461del
ENST00000638186.1:n.291del
ENST00000638360.1:n.225del
ENST00000638925.1:n.224del
ENST00000650539.1:n.393del
ENST00000330775.9:c.-13del	ENSP00000476242.2:n.-13del
ENST00000357590.9:c.-13del	ENSP00000476176.2:n.-13del
ENST00000525039.5:n.411del
ENST00000525102.5:n.745del
ENST00000525787.1:n.283del
ENST00000526626.6:n.183del
ENST00000527992.5:n.215del
ENST00000529510.5:n.6del
ENST00000530407.5:n.197+10del
ENST00000532085.1:n.1482del
ENST00000532888.6:n.183del
ENST00000534384.1:n.208del
ENST00000538950.5:c.-172+10del	ENSP00000475991.2:n.-172+10del
ENST00000545985.5:c.-13del	ENSP00000475241.2:n.-13del
NM_001164277.1:c.-13del , LRG_187t1:c.-13del	NP_001157749.1:n.-13del
NM_001164278.1:c.-13del	NP_001157750.1:n.-13del
NM_001164279.1:c.-172+10del	NP_001157751.1:n.-172+10del
NM_001164280.1:c.-13del	NP_001157752.1:n.-13del
NM_001467.5:c.-13del	NP_001458.1:n.-13del
NM_001164278.2:c.-13del	NP_001157750.1:n.-13del
NM_001164279.2:c.-172+10del	NP_001157751.1:n.-172+10del
NM_001164280.2:c.-13del	NP_001157752.1:n.-13del
NM_001467.6:c.-13del	NP_001458.1:n.-13del
NM_001164277.2:c.-13del MANE Select	NP_001157749.1:n.-13del