Canonical Allele Identifier: CA2003748571

Gene: SLC37A4

Linked Data

• dbSNP Id: rs1943536728

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025530C>T , CM000673.2:g.119025530C>T	GRCh38
NC_000011.9:g.118896240C>T , CM000673.1:g.118896240C>T	GRCh37
NC_000011.8:g.118401450C>T	NCBI36
NG_013331.1:g.10376G>A , LRG_187:g.10376G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1194+162G>A
ENST00000697845.1:n.2183+162G>A
ENST00000697846.1:n.1356G>A
ENST00000697847.1:n.1267+162G>A
ENST00000697848.1:n.1442G>A
ENST00000697849.1:n.3460G>A
ENST00000697850.1:n.1651G>A
ENST00000697851.1:n.2823-201G>A
ENST00000638186.1:n.1289-201G>A
ENST00000638360.1:n.1121-201G>A
ENST00000638925.1:n.1254-201G>A
ENST00000650539.1:n.1456+162G>A
ENST00000330775.9:c.985-201G>A	ENSP00000476242.2:n.985-201G>A
ENST00000357590.9:c.1050+162G>A	ENSP00000476176.2:n.1050+162G>A
ENST00000524428.5:n.1221-201G>A
ENST00000525039.5:n.1474+162G>A
ENST00000525102.5:n.1743-201G>A
ENST00000525372.5:n.1083-201G>A
ENST00000526275.5:n.1767-201G>A
ENST00000527992.5:n.1213-201G>A
ENST00000529510.5:n.673-201G>A
ENST00000530407.5:n.1135-201G>A
ENST00000532085.1:n.4802G>A
ENST00000538950.5:c.766-201G>A	ENSP00000475991.2:n.766-201G>A
ENST00000545985.5:c.985-201G>A	ENSP00000475241.2:n.985-201G>A
NM_001164277.1:c.985-201G>A , LRG_187t1:c.985-201G>A	NP_001157749.1:n.985-201G>A
NM_001164278.1:c.1050+162G>A	NP_001157750.1:n.1050+162G>A
NM_001164279.1:c.766-201G>A	NP_001157751.1:n.766-201G>A
NM_001164280.1:c.985-201G>A	NP_001157752.1:n.985-201G>A
NM_001467.5:c.985-201G>A	NP_001458.1:n.985-201G>A
NM_001164278.2:c.1050+162G>A	NP_001157750.1:n.1050+162G>A
NM_001164279.2:c.766-201G>A	NP_001157751.1:n.766-201G>A
NM_001164280.2:c.985-201G>A	NP_001157752.1:n.985-201G>A
NM_001467.6:c.985-201G>A	NP_001458.1:n.985-201G>A
NM_001164277.2:c.985-201G>A MANE Select	NP_001157749.1:n.985-201G>A