Canonical Allele Identifier: CA2003749129

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026618G= , CM000673.2:g.119026618G=	GRCh38
NC_000011.9:g.118897328G= , CM000673.1:g.118897328G=	GRCh37
NC_000011.8:g.118402538G=	NCBI36
NG_013331.1:g.9288C= , LRG_187:g.9288C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1014+319C=
ENST00000697845.1:n.1257C=
ENST00000697846.1:n.1014+319C=
ENST00000697847.1:n.1085C=
ENST00000697848.1:n.1085C=
ENST00000697849.1:n.2372C=
ENST00000697850.1:n.1085C=
ENST00000697851.1:n.2693C=
ENST00000638186.1:n.1159C=
ENST00000638360.1:n.991C=
ENST00000638925.1:n.1092C=
ENST00000650539.1:n.1261C=
ENST00000330775.9:c.855C=	ENSP00000476242.2:p.Asp285=
ENST00000357590.9:c.855C=	ENSP00000476176.2:p.Asp285=
ENST00000524428.5:n.1106+319C=
ENST00000525039.5:n.1279C=
ENST00000525102.5:n.1613C=
ENST00000525372.5:n.856C=
ENST00000526275.5:n.1637C=
ENST00000527992.5:n.1083C=
ENST00000529510.5:n.558+319C=
ENST00000530407.5:n.1005C=
ENST00000532085.1:n.3714C=
ENST00000538950.5:c.636C=	ENSP00000475991.2:p.Asp212=
ENST00000545985.5:c.855C=	ENSP00000475241.2:p.Asp285=
NM_001164277.1:c.855C= , LRG_187t1:c.855C=	NP_001157749.1:p.Asp285=
NM_001164278.1:c.855C=	NP_001157750.1:p.Asp285=
NM_001164279.1:c.636C=	NP_001157751.1:p.Asp212=
NM_001164280.1:c.855C=	NP_001157752.1:p.Asp285=
NM_001467.5:c.855C=	NP_001458.1:p.Asp285=
NM_001164278.2:c.855C=	NP_001157750.1:p.Asp285=
NM_001164279.2:c.636C=	NP_001157751.1:p.Asp212=
NM_001164280.2:c.855C=	NP_001157752.1:p.Asp285=
NM_001467.6:c.855C=	NP_001458.1:p.Asp285=
NM_001164277.2:c.855C= MANE Select	NP_001157749.1:p.Asp285=