Canonical Allele Identifier: CA2003748688

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025776G= , CM000673.2:g.119025776G=	GRCh38
NC_000011.9:g.118896486G= , CM000673.1:g.118896486G=	GRCh37
NC_000011.8:g.118401696G=	NCBI36
NG_013331.1:g.10130C= , LRG_187:g.10130C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1129-19C=
ENST00000697845.1:n.2099C=
ENST00000697846.1:n.1129-19C=
ENST00000697847.1:n.1202-19C=
ENST00000697848.1:n.1215-19C=
ENST00000697849.1:n.3214C=
ENST00000697850.1:n.1405C=
ENST00000697851.1:n.2822+191C=
ENST00000638186.1:n.1288+191C=
ENST00000638360.1:n.1120+191C=
ENST00000638925.1:n.1253+191C=
ENST00000650539.1:n.1391-19C=
ENST00000330775.9:c.984+191C=	ENSP00000476242.2:n.984+191C=
ENST00000357590.9:c.985-19C=	ENSP00000476176.2:n.985-19C=
ENST00000524428.5:n.1220+191C=
ENST00000525039.5:n.1409-19C=
ENST00000525102.5:n.1742+191C=
ENST00000525372.5:n.1082+191C=
ENST00000526275.5:n.1766+191C=
ENST00000527992.5:n.1212+191C=
ENST00000529510.5:n.672+191C=
ENST00000530407.5:n.1134+191C=
ENST00000532085.1:n.4556C=
ENST00000538950.5:c.765+191C=	ENSP00000475991.2:n.765+191C=
ENST00000545985.5:c.984+191C=	ENSP00000475241.2:n.984+191C=
NM_001164277.1:c.984+191C= , LRG_187t1:c.984+191C=	NP_001157749.1:n.984+191C=
NM_001164278.1:c.985-19C=	NP_001157750.1:n.985-19C=
NM_001164279.1:c.765+191C=	NP_001157751.1:n.765+191C=
NM_001164280.1:c.984+191C=	NP_001157752.1:n.984+191C=
NM_001467.5:c.984+191C=	NP_001458.1:n.984+191C=
NM_001164278.2:c.985-19C=	NP_001157750.1:n.985-19C=
NM_001164279.2:c.765+191C=	NP_001157751.1:n.765+191C=
NM_001164280.2:c.984+191C=	NP_001157752.1:n.984+191C=
NM_001467.6:c.984+191C=	NP_001458.1:n.984+191C=
NM_001164277.2:c.984+191C= MANE Select	NP_001157749.1:n.984+191C=