Canonical Allele Identifier: CA2616340768

Gene: SLC37A4

Linked Data

• gnomAD v4: 11-119029512-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029512C>T , CM000673.2:g.119029512C>T	GRCh38
NC_000011.9:g.118900222C>T , CM000673.1:g.118900222C>T	GRCh37
NC_000011.8:g.118405432C>T	NCBI36
NG_013331.1:g.6395G>A , LRG_187:g.6395G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.87G>A
ENST00000697846.1:n.87G>A
ENST00000697847.1:n.87G>A
ENST00000697848.1:n.87G>A
ENST00000697849.1:n.331G>A
ENST00000697850.1:n.87G>A
ENST00000697851.1:n.331G>A
ENST00000638186.1:n.161G>A
ENST00000638360.1:n.95G>A
ENST00000638925.1:n.94G>A
ENST00000650539.1:n.263G>A
ENST00000330775.9:c.-143G>A	ENSP00000476242.2:n.-143G>A
ENST00000357590.9:c.-143G>A	ENSP00000476176.2:n.-143G>A
ENST00000525039.5:n.281G>A
ENST00000525102.5:n.615G>A
ENST00000525787.1:n.153G>A
ENST00000526626.6:n.53G>A
ENST00000527992.5:n.85G>A
ENST00000530407.5:n.77G>A
ENST00000532085.1:n.1352G>A
ENST00000532888.6:n.53G>A
ENST00000534384.1:n.78G>A
ENST00000538950.5:c.-292G>A	ENSP00000475991.2:n.-292G>A
ENST00000545985.5:c.-143G>A	ENSP00000475241.2:n.-143G>A
NM_001164277.1:c.-143G>A , LRG_187t1:c.-143G>A	NP_001157749.1:n.-143G>A
NM_001164278.1:c.-143G>A	NP_001157750.1:n.-143G>A
NM_001164279.1:c.-292G>A	NP_001157751.1:n.-292G>A
NM_001164280.1:c.-143G>A	NP_001157752.1:n.-143G>A
NM_001467.5:c.-143G>A	NP_001458.1:n.-143G>A
NM_001164278.2:c.-143G>A	NP_001157750.1:n.-143G>A
NM_001164279.2:c.-292G>A	NP_001157751.1:n.-292G>A
NM_001467.6:c.-143G>A	NP_001458.1:n.-143G>A
NM_001164277.2:c.-143G>A MANE Select	NP_001157749.1:n.-143G>A