Canonical Allele Identifier: CA2003749105

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026575C= , CM000673.2:g.119026575C=	GRCh38
NC_000011.9:g.118897285C= , CM000673.1:g.118897285C=	GRCh37
NC_000011.8:g.118402495C=	NCBI36
NG_013331.1:g.9331G= , LRG_187:g.9331G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.1014+362G=
ENST00000697845.1:n.1300G=
ENST00000697846.1:n.1014+362G=
ENST00000697847.1:n.1128G=
ENST00000697848.1:n.1100+28G=
ENST00000697849.1:n.2415G=
ENST00000697850.1:n.1100+28G=
ENST00000697851.1:n.2708+28G=
ENST00000638186.1:n.1174+28G=
ENST00000638360.1:n.1006+28G=
ENST00000638925.1:n.1135G=
ENST00000650539.1:n.1276+28G=
ENST00000330775.9:c.870+28G=	ENSP00000476242.2:n.870+28G=
ENST00000357590.9:c.870+28G=	ENSP00000476176.2:n.870+28G=
ENST00000524428.5:n.1106+362G=
ENST00000525039.5:n.1294+28G=
ENST00000525102.5:n.1628+28G=
ENST00000525372.5:n.899G=
ENST00000526275.5:n.1652+28G=
ENST00000527992.5:n.1098+28G=
ENST00000529510.5:n.558+362G=
ENST00000530407.5:n.1020+28G=
ENST00000532085.1:n.3757G=
ENST00000538950.5:c.651+28G=	ENSP00000475991.2:n.651+28G=
ENST00000545985.5:c.870+28G=	ENSP00000475241.2:n.870+28G=
NM_001164277.1:c.870+28G= , LRG_187t1:c.870+28G=	NP_001157749.1:n.870+28G=
NM_001164278.1:c.870+28G=	NP_001157750.1:n.870+28G=
NM_001164279.1:c.651+28G=	NP_001157751.1:n.651+28G=
NM_001164280.1:c.870+28G=	NP_001157752.1:n.870+28G=
NM_001467.5:c.870+28G=	NP_001458.1:n.870+28G=
NM_001164278.2:c.870+28G=	NP_001157750.1:n.870+28G=
NM_001164279.2:c.651+28G=	NP_001157751.1:n.651+28G=
NM_001164280.2:c.870+28G=	NP_001157752.1:n.870+28G=
NM_001467.6:c.870+28G=	NP_001458.1:n.870+28G=
NM_001164277.2:c.870+28G= MANE Select	NP_001157749.1:n.870+28G=