Canonical Allele Identifier: CA2616340712

Gene: SLC37A4

Linked Data

• gnomAD v4: 11-119029457-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029457G>C , CM000673.2:g.119029457G>C	GRCh38
NC_000011.9:g.118900167G>C , CM000673.1:g.118900167G>C	GRCh37
NC_000011.8:g.118405377G>C	NCBI36
NG_013331.1:g.6450C>G , LRG_187:g.6450C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.142C>G
ENST00000697846.1:n.142C>G
ENST00000697847.1:n.142C>G
ENST00000697848.1:n.142C>G
ENST00000697849.1:n.386C>G
ENST00000697850.1:n.142C>G
ENST00000697851.1:n.386C>G
ENST00000638186.1:n.216C>G
ENST00000638360.1:n.150C>G
ENST00000638925.1:n.149C>G
ENST00000650539.1:n.318C>G
ENST00000330775.9:c.-88C>G	ENSP00000476242.2:n.-88C>G
ENST00000357590.9:c.-88C>G	ENSP00000476176.2:n.-88C>G
ENST00000525039.5:n.336C>G
ENST00000525102.5:n.670C>G
ENST00000525787.1:n.208C>G
ENST00000526626.6:n.108C>G
ENST00000527992.5:n.140C>G
ENST00000530407.5:n.132C>G
ENST00000532085.1:n.1407C>G
ENST00000532888.6:n.108C>G
ENST00000534384.1:n.133C>G
ENST00000538950.5:c.-237C>G	ENSP00000475991.2:n.-237C>G
ENST00000545985.5:c.-88C>G	ENSP00000475241.2:n.-88C>G
NM_001164277.1:c.-88C>G , LRG_187t1:c.-88C>G	NP_001157749.1:n.-88C>G
NM_001164278.1:c.-88C>G	NP_001157750.1:n.-88C>G
NM_001164279.1:c.-237C>G	NP_001157751.1:n.-237C>G
NM_001164280.1:c.-88C>G	NP_001157752.1:n.-88C>G
NM_001467.5:c.-88C>G	NP_001458.1:n.-88C>G
NM_001164278.2:c.-88C>G	NP_001157750.1:n.-88C>G
NM_001164279.2:c.-237C>G	NP_001157751.1:n.-237C>G
NM_001164280.2:c.-88C>G	NP_001157752.1:n.-88C>G
NM_001467.6:c.-88C>G	NP_001458.1:n.-88C>G
NM_001164277.2:c.-88C>G MANE Select	NP_001157749.1:n.-88C>G