Canonical Allele Identifier: CA2003775984

Gene: SLC37A4

Linked Data

• dbSNP Id: rs1943697516
• gnomAD v4: 11-119029926-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029926C>A , CM000673.2:g.119029926C>A	GRCh38
NC_000011.9:g.118900636C>A , CM000673.1:g.118900636C>A	GRCh37
NC_000011.8:g.118405846C>A	NCBI36
NG_013331.1:g.5981G>T , LRG_187:g.5981G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.35-362G>T
ENST00000697846.1:n.35-362G>T
ENST00000697847.1:n.35-362G>T
ENST00000697848.1:n.35-362G>T
ENST00000697850.1:n.35-362G>T
ENST00000638186.1:n.49G>T
ENST00000638360.1:n.43-362G>T
ENST00000638925.1:n.42-362G>T
ENST00000650539.1:n.210+244G>T
ENST00000330775.9:c.-195-362G>T	ENSP00000476242.2:n.-195-362G>T
ENST00000357590.9:c.-195-362G>T	ENSP00000476176.2:n.-195-362G>T
ENST00000525039.5:n.229-362G>T
ENST00000525102.5:n.562+306G>T
ENST00000527992.5:n.33-362G>T
ENST00000530407.5:n.25-362G>T
ENST00000532085.1:n.938G>T
ENST00000534384.1:n.15G>T
ENST00000538950.5:c.-344-362G>T	ENSP00000475991.2:n.-344-362G>T
ENST00000545985.5:c.-196+306G>T	ENSP00000475241.2:n.-196+306G>T
NM_001164277.1:c.-196+306G>T , LRG_187t1:c.-196+306G>T	NP_001157749.1:n.-196+306G>T
NM_001164278.1:c.-195-362G>T	NP_001157750.1:n.-195-362G>T
NM_001164279.1:c.-344-362G>T	NP_001157751.1:n.-344-362G>T
NM_001467.5:c.-195-362G>T	NP_001458.1:n.-195-362G>T
NM_001164278.2:c.-195-362G>T	NP_001157750.1:n.-195-362G>T
NM_001164279.2:c.-344-362G>T	NP_001157751.1:n.-344-362G>T
NM_001467.6:c.-195-362G>T	NP_001458.1:n.-195-362G>T
NM_001164277.2:c.-196+306G>T MANE Select	NP_001157749.1:n.-196+306G>T