Canonical Allele Identifier: CA2003774606

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119028938C= , CM000673.2:g.119028938C=	GRCh38
NC_000011.9:g.118899648C= , CM000673.1:g.118899648C=	GRCh37
NC_000011.8:g.118404858C=	NCBI36
NG_013331.1:g.6969G= , LRG_187:g.6969G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.377+284G=
ENST00000697846.1:n.377+284G=
ENST00000697847.1:n.377+284G=
ENST00000697848.1:n.377+284G=
ENST00000697849.1:n.905G=
ENST00000697850.1:n.377+284G=
ENST00000697851.1:n.905G=
ENST00000638186.1:n.451+284G=
ENST00000638360.1:n.385+284G=
ENST00000638925.1:n.384+284G=
ENST00000650539.1:n.553+284G=
ENST00000330775.9:c.148+284G=	ENSP00000476242.2:n.148+284G=
ENST00000357590.9:c.148+284G=	ENSP00000476176.2:n.148+284G=
ENST00000524428.5:n.148+284G=
ENST00000525039.5:n.571+284G=
ENST00000525102.5:n.905+284G=
ENST00000525372.5:n.148+284G=
ENST00000525787.1:n.443+284G=
ENST00000526275.5:n.97G=
ENST00000526626.6:n.343+284G=
ENST00000527992.5:n.375+284G=
ENST00000529510.5:n.166+284G=
ENST00000530407.5:n.198-104G=
ENST00000532085.1:n.1926G=
ENST00000532888.6:n.344-104G=
ENST00000534384.1:n.368+284G=
ENST00000538950.5:c.-171-104G=	ENSP00000475991.2:n.-171-104G=
ENST00000545985.5:c.148+284G=	ENSP00000475241.2:n.148+284G=
NM_001164277.1:c.148+284G= , LRG_187t1:c.148+284G=	NP_001157749.1:n.148+284G=
NM_001164278.1:c.148+284G=	NP_001157750.1:n.148+284G=
NM_001164279.1:c.-171-104G=	NP_001157751.1:n.-171-104G=
NM_001164280.1:c.148+284G=	NP_001157752.1:n.148+284G=
NM_001467.5:c.148+284G=	NP_001458.1:n.148+284G=
NM_001164278.2:c.148+284G=	NP_001157750.1:n.148+284G=
NM_001164279.2:c.-171-104G=	NP_001157751.1:n.-171-104G=
NM_001164280.2:c.148+284G=	NP_001157752.1:n.148+284G=
NM_001467.6:c.148+284G=	NP_001458.1:n.148+284G=
NM_001164277.2:c.148+284G= MANE Select	NP_001157749.1:n.148+284G=