Canonical Allele Identifier: CA2616340798

Gene: SLC37A4

Linked Data

• gnomAD v4: 11-119029548-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029548C>A , CM000673.2:g.119029548C>A	GRCh38
NC_000011.9:g.118900258C>A , CM000673.1:g.118900258C>A	GRCh37
NC_000011.8:g.118405468C>A	NCBI36
NG_013331.1:g.6359G>T , LRG_187:g.6359G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.51G>T
ENST00000697846.1:n.51G>T
ENST00000697847.1:n.51G>T
ENST00000697848.1:n.51G>T
ENST00000697849.1:n.295G>T
ENST00000697850.1:n.51G>T
ENST00000697851.1:n.295G>T
ENST00000638186.1:n.125G>T
ENST00000638360.1:n.59G>T
ENST00000638925.1:n.58G>T
ENST00000650539.1:n.227G>T
ENST00000330775.9:c.-179G>T	ENSP00000476242.2:n.-179G>T
ENST00000357590.9:c.-179G>T	ENSP00000476176.2:n.-179G>T
ENST00000525039.5:n.245G>T
ENST00000525102.5:n.579G>T
ENST00000525787.1:n.117G>T
ENST00000526626.6:n.17G>T
ENST00000527992.5:n.49G>T
ENST00000530407.5:n.41G>T
ENST00000532085.1:n.1316G>T
ENST00000532888.6:n.17G>T
ENST00000534384.1:n.42G>T
ENST00000538950.5:c.-328G>T	ENSP00000475991.2:n.-328G>T
ENST00000545985.5:c.-179G>T	ENSP00000475241.2:n.-179G>T
NM_001164277.1:c.-179G>T , LRG_187t1:c.-179G>T	NP_001157749.1:n.-179G>T
NM_001164278.1:c.-179G>T	NP_001157750.1:n.-179G>T
NM_001164279.1:c.-328G>T	NP_001157751.1:n.-328G>T
NM_001164280.1:c.-179G>T	NP_001157752.1:n.-179G>T
NM_001467.5:c.-179G>T	NP_001458.1:n.-179G>T
NM_001164278.2:c.-179G>T	NP_001157750.1:n.-179G>T
NM_001164279.2:c.-328G>T	NP_001157751.1:n.-328G>T
NM_001467.6:c.-179G>T	NP_001458.1:n.-179G>T
NM_001164277.2:c.-179G>T MANE Select	NP_001157749.1:n.-179G>T