Canonical Allele Identifier: CA382897266

Gene: SLC37A4

Linked Data

• MyVariant Identifiers: chr11:g.118896699G>T (hg19) ; chr11:g.119025989G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025989G>T , CM000673.2:g.119025989G>T	GRCh38
NC_000011.9:g.118896699G>T , CM000673.1:g.118896699G>T	GRCh37
NC_000011.8:g.118401909G>T	NCBI36
NG_013331.1:g.9917C>A , LRG_187:g.9917C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1106C>A
ENST00000697845.1:n.1886C>A
ENST00000697846.1:n.1106C>A
ENST00000697847.1:n.1202-232C>A
ENST00000697848.1:n.1192C>A
ENST00000697849.1:n.3001C>A
ENST00000697850.1:n.1192C>A
ENST00000697851.1:n.2800C>A
ENST00000638186.1:n.1266C>A
ENST00000638360.1:n.1098C>A
ENST00000638925.1:n.1231C>A
ENST00000650539.1:n.1368C>A
ENST00000330775.9:c.962C>A	ENSP00000476242.2:p.Thr321Lys
ENST00000357590.9:c.962C>A	ENSP00000476176.2:p.Thr321Lys
ENST00000524428.5:n.1198C>A
ENST00000525039.5:n.1386C>A
ENST00000525102.5:n.1720C>A
ENST00000525372.5:n.1060C>A
ENST00000526275.5:n.1744C>A
ENST00000527992.5:n.1190C>A
ENST00000529510.5:n.650C>A
ENST00000530407.5:n.1112C>A
ENST00000532085.1:n.4343C>A
ENST00000538950.5:c.743C>A	ENSP00000475991.2:p.Thr248Lys
ENST00000545985.5:c.962C>A	ENSP00000475241.2:p.Thr321Lys
NM_001164277.1:c.962C>A , LRG_187t1:c.962C>A	NP_001157749.1:p.Thr321Lys
NM_001164278.1:c.962C>A	NP_001157750.1:p.Thr321Lys
NM_001164279.1:c.743C>A	NP_001157751.1:p.Thr248Lys
NM_001164280.1:c.962C>A	NP_001157752.1:p.Thr321Lys
NM_001467.5:c.962C>A	NP_001458.1:p.Thr321Lys
NM_001164278.2:c.962C>A	NP_001157750.1:p.Thr321Lys
NM_001164279.2:c.743C>A	NP_001157751.1:p.Thr248Lys
NM_001164280.2:c.962C>A	NP_001157752.1:p.Thr321Lys
NM_001467.6:c.962C>A	NP_001458.1:p.Thr321Lys
NM_001164277.2:c.962C>A MANE Select	NP_001157749.1:p.Thr321Lys