Canonical Allele Identifier: CA2003749725

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027766T= , CM000673.2:g.119027766T=	GRCh38
NC_000011.9:g.118898476T= , CM000673.1:g.118898476T=	GRCh37
NC_000011.8:g.118403686T=	NCBI36
NG_013331.1:g.8141A= , LRG_187:g.8141A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.717A=
ENST00000697845.1:n.641A=
ENST00000697846.1:n.717A=
ENST00000697847.1:n.717A=
ENST00000697848.1:n.717A=
ENST00000697849.1:n.1756A=
ENST00000697850.1:n.717A=
ENST00000697851.1:n.2077A=
ENST00000638186.1:n.791A=
ENST00000638360.1:n.623A=
ENST00000638925.1:n.724A=
ENST00000650539.1:n.893A=
ENST00000330775.9:c.488A=	ENSP00000476242.2:p.Tyr163=
ENST00000357590.9:c.488A=	ENSP00000476176.2:p.Tyr163=
ENST00000524428.5:n.809A=
ENST00000525039.5:n.911A=
ENST00000525102.5:n.1245A=
ENST00000525372.5:n.488A=
ENST00000526275.5:n.1269A=
ENST00000526626.6:n.450A=
ENST00000527992.5:n.715A=
ENST00000529510.5:n.399+428A=
ENST00000530407.5:n.637A=
ENST00000532085.1:n.3098A=
ENST00000532888.6:n.783A=
ENST00000538950.5:c.269A=	ENSP00000475991.2:p.Tyr90=
ENST00000545985.5:c.488A=	ENSP00000475241.2:p.Tyr163=
NM_001164277.1:c.488A= , LRG_187t1:c.488A=	NP_001157749.1:p.Tyr163=
NM_001164278.1:c.488A=	NP_001157750.1:p.Tyr163=
NM_001164279.1:c.269A=	NP_001157751.1:p.Tyr90=
NM_001164280.1:c.488A=	NP_001157752.1:p.Tyr163=
NM_001467.5:c.488A=	NP_001458.1:p.Tyr163=
NM_001164278.2:c.488A=	NP_001157750.1:p.Tyr163=
NM_001164279.2:c.269A=	NP_001157751.1:p.Tyr90=
NM_001164280.2:c.488A=	NP_001157752.1:p.Tyr163=
NM_001467.6:c.488A=	NP_001458.1:p.Tyr163=
NM_001164277.2:c.488A= MANE Select	NP_001157749.1:p.Tyr163=