Canonical Allele Identifier: CA229601393

Gene: SLC37A4

Linked Data

• dbSNP Id: rs1038962428
• gnomAD v3: 11-119029464-GT-G
• gnomAD v4: 11-119029464-GT-G
• MyVariant Identifiers: chr11:g.118900175del (hg19) ; chr11:g.119029465del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029470del , CM000673.2:g.119029470del	GRCh38
NC_000011.9:g.118900180del , CM000673.1:g.118900180del	GRCh37
NC_000011.8:g.118405390del	NCBI36
NG_013331.1:g.6442del , LRG_187:g.6442del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.134del
ENST00000697846.1:n.134del
ENST00000697847.1:n.134del
ENST00000697848.1:n.134del
ENST00000697849.1:n.378del
ENST00000697850.1:n.134del
ENST00000697851.1:n.378del
ENST00000638186.1:n.208del
ENST00000638360.1:n.142del
ENST00000638925.1:n.141del
ENST00000650539.1:n.310del
ENST00000330775.9:c.-96del	ENSP00000476242.2:n.-96del
ENST00000357590.9:c.-96del	ENSP00000476176.2:n.-96del
ENST00000525039.5:n.328del
ENST00000525102.5:n.662del
ENST00000525787.1:n.200del
ENST00000526626.6:n.100del
ENST00000527992.5:n.132del
ENST00000530407.5:n.124del
ENST00000532085.1:n.1399del
ENST00000532888.6:n.100del
ENST00000534384.1:n.125del
ENST00000538950.5:c.-245del	ENSP00000475991.2:n.-245del
ENST00000545985.5:c.-96del	ENSP00000475241.2:n.-96del
NM_001164277.1:c.-96del , LRG_187t1:c.-96del	NP_001157749.1:n.-96del
NM_001164278.1:c.-96del	NP_001157750.1:n.-96del
NM_001164279.1:c.-245del	NP_001157751.1:n.-245del
NM_001164280.1:c.-96del	NP_001157752.1:n.-96del
NM_001467.5:c.-96del	NP_001458.1:n.-96del
NM_001164278.2:c.-96del	NP_001157750.1:n.-96del
NM_001164279.2:c.-245del	NP_001157751.1:n.-245del
NM_001164280.2:c.-96del	NP_001157752.1:n.-96del
NM_001467.6:c.-96del	NP_001458.1:n.-96del
NM_001164277.2:c.-96del MANE Select	NP_001157749.1:n.-96del