Canonical Allele Identifier: CA2003748662

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025733G= , CM000673.2:g.119025733G=	GRCh38
NC_000011.9:g.118896443G= , CM000673.1:g.118896443G=	GRCh37
NC_000011.8:g.118401653G=	NCBI36
NG_013331.1:g.10173C= , LRG_187:g.10173C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1153C=
ENST00000697845.1:n.2142C=
ENST00000697846.1:n.1153C=
ENST00000697847.1:n.1226C=
ENST00000697848.1:n.1239C=
ENST00000697849.1:n.3257C=
ENST00000697850.1:n.1448C=
ENST00000697851.1:n.2822+234C=
ENST00000638186.1:n.1288+234C=
ENST00000638360.1:n.1120+234C=
ENST00000638925.1:n.1253+234C=
ENST00000650539.1:n.1415C=
ENST00000330775.9:c.984+234C=	ENSP00000476242.2:n.984+234C=
ENST00000357590.9:c.1009C=	ENSP00000476176.2:p.Leu337=
ENST00000524428.5:n.1220+234C=
ENST00000525039.5:n.1433C=
ENST00000525102.5:n.1742+234C=
ENST00000525372.5:n.1082+234C=
ENST00000526275.5:n.1766+234C=
ENST00000527992.5:n.1212+234C=
ENST00000529510.5:n.672+234C=
ENST00000530407.5:n.1134+234C=
ENST00000532085.1:n.4599C=
ENST00000538950.5:c.765+234C=	ENSP00000475991.2:n.765+234C=
ENST00000545985.5:c.984+234C=	ENSP00000475241.2:n.984+234C=
NM_001164277.1:c.984+234C= , LRG_187t1:c.984+234C=	NP_001157749.1:n.984+234C=
NM_001164278.1:c.1009C=	NP_001157750.1:p.Leu337=
NM_001164279.1:c.765+234C=	NP_001157751.1:n.765+234C=
NM_001164280.1:c.984+234C=	NP_001157752.1:n.984+234C=
NM_001467.5:c.984+234C=	NP_001458.1:n.984+234C=
NM_001164278.2:c.1009C=	NP_001157750.1:p.Leu337=
NM_001164279.2:c.765+234C=	NP_001157751.1:n.765+234C=
NM_001164280.2:c.984+234C=	NP_001157752.1:n.984+234C=
NM_001467.6:c.984+234C=	NP_001458.1:n.984+234C=
NM_001164277.2:c.984+234C= MANE Select	NP_001157749.1:n.984+234C=