Canonical Allele Identifier: CA2003775363

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029398A= , CM000673.2:g.119029398A=	GRCh38
NC_000011.9:g.118900108A= , CM000673.1:g.118900108A=	GRCh37
NC_000011.8:g.118405318A=	NCBI36
NG_013331.1:g.6509T= , LRG_187:g.6509T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.201T=
ENST00000697846.1:n.201T=
ENST00000697847.1:n.201T=
ENST00000697848.1:n.201T=
ENST00000697849.1:n.445T=
ENST00000697850.1:n.201T=
ENST00000697851.1:n.445T=
ENST00000638186.1:n.275T=
ENST00000638360.1:n.209T=
ENST00000638925.1:n.208T=
ENST00000650539.1:n.377T=
ENST00000330775.9:c.-29T=	ENSP00000476242.2:n.-29T=
ENST00000357590.9:c.-29T=	ENSP00000476176.2:n.-29T=
ENST00000525039.5:n.395T=
ENST00000525102.5:n.729T=
ENST00000525787.1:n.267T=
ENST00000526626.6:n.167T=
ENST00000527992.5:n.199T=
ENST00000530407.5:n.191T=
ENST00000532085.1:n.1466T=
ENST00000532888.6:n.167T=
ENST00000534384.1:n.192T=
ENST00000538950.5:c.-178T=	ENSP00000475991.2:n.-178T=
ENST00000545985.5:c.-29T=	ENSP00000475241.2:n.-29T=
NM_001164277.1:c.-29T= , LRG_187t1:c.-29T=	NP_001157749.1:n.-29T=
NM_001164278.1:c.-29T=	NP_001157750.1:n.-29T=
NM_001164279.1:c.-178T=	NP_001157751.1:n.-178T=
NM_001164280.1:c.-29T=	NP_001157752.1:n.-29T=
NM_001467.5:c.-29T=	NP_001458.1:n.-29T=
NM_001164278.2:c.-29T=	NP_001157750.1:n.-29T=
NM_001164279.2:c.-178T=	NP_001157751.1:n.-178T=
NM_001164280.2:c.-29T=	NP_001157752.1:n.-29T=
NM_001467.6:c.-29T=	NP_001458.1:n.-29T=
NM_001164277.2:c.-29T= MANE Select	NP_001157749.1:n.-29T=