Canonical Allele Identifier: CA2616340695

Gene: SLC37A4

Linked Data

• gnomAD v4: 11-119029437-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029437T>C , CM000673.2:g.119029437T>C	GRCh38
NC_000011.9:g.118900147T>C , CM000673.1:g.118900147T>C	GRCh37
NC_000011.8:g.118405357T>C	NCBI36
NG_013331.1:g.6470A>G , LRG_187:g.6470A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.162A>G
ENST00000697846.1:n.162A>G
ENST00000697847.1:n.162A>G
ENST00000697848.1:n.162A>G
ENST00000697849.1:n.406A>G
ENST00000697850.1:n.162A>G
ENST00000697851.1:n.406A>G
ENST00000638186.1:n.236A>G
ENST00000638360.1:n.170A>G
ENST00000638925.1:n.169A>G
ENST00000650539.1:n.338A>G
ENST00000330775.9:c.-68A>G	ENSP00000476242.2:n.-68A>G
ENST00000357590.9:c.-68A>G	ENSP00000476176.2:n.-68A>G
ENST00000525039.5:n.356A>G
ENST00000525102.5:n.690A>G
ENST00000525787.1:n.228A>G
ENST00000526626.6:n.128A>G
ENST00000527992.5:n.160A>G
ENST00000530407.5:n.152A>G
ENST00000532085.1:n.1427A>G
ENST00000532888.6:n.128A>G
ENST00000534384.1:n.153A>G
ENST00000538950.5:c.-217A>G	ENSP00000475991.2:n.-217A>G
ENST00000545985.5:c.-68A>G	ENSP00000475241.2:n.-68A>G
NM_001164277.1:c.-68A>G , LRG_187t1:c.-68A>G	NP_001157749.1:n.-68A>G
NM_001164278.1:c.-68A>G	NP_001157750.1:n.-68A>G
NM_001164279.1:c.-217A>G	NP_001157751.1:n.-217A>G
NM_001164280.1:c.-68A>G	NP_001157752.1:n.-68A>G
NM_001467.5:c.-68A>G	NP_001458.1:n.-68A>G
NM_001164278.2:c.-68A>G	NP_001157750.1:n.-68A>G
NM_001164279.2:c.-217A>G	NP_001157751.1:n.-217A>G
NM_001164280.2:c.-68A>G	NP_001157752.1:n.-68A>G
NM_001467.6:c.-68A>G	NP_001458.1:n.-68A>G
NM_001164277.2:c.-68A>G MANE Select	NP_001157749.1:n.-68A>G