Canonical Allele Identifier: CA2003748751

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025878C= , CM000673.2:g.119025878C=	GRCh38
NC_000011.9:g.118896588C= , CM000673.1:g.118896588C=	GRCh37
NC_000011.8:g.118401798C=	NCBI36
NG_013331.1:g.10028G= , LRG_187:g.10028G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1128+89G=
ENST00000697845.1:n.1997G=
ENST00000697846.1:n.1128+89G=
ENST00000697847.1:n.1202-121G=
ENST00000697848.1:n.1214+89G=
ENST00000697849.1:n.3112G=
ENST00000697850.1:n.1303G=
ENST00000697851.1:n.2822+89G=
ENST00000638186.1:n.1288+89G=
ENST00000638360.1:n.1120+89G=
ENST00000638925.1:n.1253+89G=
ENST00000650539.1:n.1390+89G=
ENST00000330775.9:c.984+89G=	ENSP00000476242.2:n.984+89G=
ENST00000357590.9:c.984+89G=	ENSP00000476176.2:n.984+89G=
ENST00000524428.5:n.1220+89G=
ENST00000525039.5:n.1408+89G=
ENST00000525102.5:n.1742+89G=
ENST00000525372.5:n.1082+89G=
ENST00000526275.5:n.1766+89G=
ENST00000527992.5:n.1212+89G=
ENST00000529510.5:n.672+89G=
ENST00000530407.5:n.1134+89G=
ENST00000532085.1:n.4454G=
ENST00000538950.5:c.765+89G=	ENSP00000475991.2:n.765+89G=
ENST00000545985.5:c.984+89G=	ENSP00000475241.2:n.984+89G=
NM_001164277.1:c.984+89G= , LRG_187t1:c.984+89G=	NP_001157749.1:n.984+89G=
NM_001164278.1:c.984+89G=	NP_001157750.1:n.984+89G=
NM_001164279.1:c.765+89G=	NP_001157751.1:n.765+89G=
NM_001164280.1:c.984+89G=	NP_001157752.1:n.984+89G=
NM_001467.5:c.984+89G=	NP_001458.1:n.984+89G=
NM_001164278.2:c.984+89G=	NP_001157750.1:n.984+89G=
NM_001164279.2:c.765+89G=	NP_001157751.1:n.765+89G=
NM_001164280.2:c.984+89G=	NP_001157752.1:n.984+89G=
NM_001467.6:c.984+89G=	NP_001458.1:n.984+89G=
NM_001164277.2:c.984+89G= MANE Select	NP_001157749.1:n.984+89G=