Canonical Allele Identifier: CA2003749529

Gene: SLC37A4

Linked Data

• dbSNP Id: rs1565688922

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027403A>C , CM000673.2:g.119027403A>C	GRCh38
NC_000011.9:g.118898113A>C , CM000673.1:g.118898113A>C	GRCh37
NC_000011.8:g.118403323A>C	NCBI36
NG_013331.1:g.8503T>G , LRG_187:g.8503T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.855+225T>G
ENST00000697845.1:n.779+225T>G
ENST00000697846.1:n.855+225T>G
ENST00000697847.1:n.855+225T>G
ENST00000697848.1:n.855+225T>G
ENST00000697849.1:n.1894+225T>G
ENST00000697850.1:n.855+225T>G
ENST00000697851.1:n.2215+225T>G
ENST00000638186.1:n.929+225T>G
ENST00000638360.1:n.761+225T>G
ENST00000638925.1:n.862+225T>G
ENST00000650539.1:n.1031+225T>G
ENST00000330775.9:c.625+225T>G	ENSP00000476242.2:n.625+225T>G
ENST00000357590.9:c.625+225T>G	ENSP00000476176.2:n.625+225T>G
ENST00000524428.5:n.947+225T>G
ENST00000525039.5:n.1049+225T>G
ENST00000525102.5:n.1383+225T>G
ENST00000525372.5:n.626+225T>G
ENST00000526275.5:n.1407+225T>G
ENST00000526626.6:n.588+225T>G
ENST00000527992.5:n.853+225T>G
ENST00000529510.5:n.400-308T>G
ENST00000530407.5:n.775+225T>G
ENST00000532085.1:n.3236+225T>G
ENST00000532888.6:n.921+225T>G
ENST00000538950.5:c.406+225T>G	ENSP00000475991.2:n.406+225T>G
ENST00000545985.5:c.625+225T>G	ENSP00000475241.2:n.625+225T>G
NM_001164277.1:c.625+225T>G , LRG_187t1:c.625+225T>G	NP_001157749.1:n.625+225T>G
NM_001164278.1:c.625+225T>G	NP_001157750.1:n.625+225T>G
NM_001164279.1:c.406+225T>G	NP_001157751.1:n.406+225T>G
NM_001164280.1:c.625+225T>G	NP_001157752.1:n.625+225T>G
NM_001467.5:c.625+225T>G	NP_001458.1:n.625+225T>G
NM_001164278.2:c.625+225T>G	NP_001157750.1:n.625+225T>G
NM_001164279.2:c.406+225T>G	NP_001157751.1:n.406+225T>G
NM_001164280.2:c.625+225T>G	NP_001157752.1:n.625+225T>G
NM_001467.6:c.625+225T>G	NP_001458.1:n.625+225T>G
NM_001164277.2:c.625+225T>G MANE Select	NP_001157749.1:n.625+225T>G