Canonical Allele Identifier: CA2616340668

Gene: SLC37A4

Linked Data

• gnomAD v4: 11-119029402-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029402G>C , CM000673.2:g.119029402G>C	GRCh38
NC_000011.9:g.118900112G>C , CM000673.1:g.118900112G>C	GRCh37
NC_000011.8:g.118405322G>C	NCBI36
NG_013331.1:g.6505C>G , LRG_187:g.6505C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.197C>G
ENST00000697846.1:n.197C>G
ENST00000697847.1:n.197C>G
ENST00000697848.1:n.197C>G
ENST00000697849.1:n.441C>G
ENST00000697850.1:n.197C>G
ENST00000697851.1:n.441C>G
ENST00000638186.1:n.271C>G
ENST00000638360.1:n.205C>G
ENST00000638925.1:n.204C>G
ENST00000650539.1:n.373C>G
ENST00000330775.9:c.-33C>G	ENSP00000476242.2:n.-33C>G
ENST00000357590.9:c.-33C>G	ENSP00000476176.2:n.-33C>G
ENST00000525039.5:n.391C>G
ENST00000525102.5:n.725C>G
ENST00000525787.1:n.263C>G
ENST00000526626.6:n.163C>G
ENST00000527992.5:n.195C>G
ENST00000530407.5:n.187C>G
ENST00000532085.1:n.1462C>G
ENST00000532888.6:n.163C>G
ENST00000534384.1:n.188C>G
ENST00000538950.5:c.-182C>G	ENSP00000475991.2:n.-182C>G
ENST00000545985.5:c.-33C>G	ENSP00000475241.2:n.-33C>G
NM_001164277.1:c.-33C>G , LRG_187t1:c.-33C>G	NP_001157749.1:n.-33C>G
NM_001164278.1:c.-33C>G	NP_001157750.1:n.-33C>G
NM_001164279.1:c.-182C>G	NP_001157751.1:n.-182C>G
NM_001164280.1:c.-33C>G	NP_001157752.1:n.-33C>G
NM_001467.5:c.-33C>G	NP_001458.1:n.-33C>G
NM_001164278.2:c.-33C>G	NP_001157750.1:n.-33C>G
NM_001164279.2:c.-182C>G	NP_001157751.1:n.-182C>G
NM_001164280.2:c.-33C>G	NP_001157752.1:n.-33C>G
NM_001467.6:c.-33C>G	NP_001458.1:n.-33C>G
NM_001164277.2:c.-33C>G MANE Select	NP_001157749.1:n.-33C>G