Canonical Allele Identifier: CA2003775458

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119029450A= , CM000673.2:g.119029450A=	GRCh38
NC_000011.9:g.118900160A= , CM000673.1:g.118900160A=	GRCh37
NC_000011.8:g.118405370A=	NCBI36
NG_013331.1:g.6457T= , LRG_187:g.6457T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.149T=
ENST00000697846.1:n.149T=
ENST00000697847.1:n.149T=
ENST00000697848.1:n.149T=
ENST00000697849.1:n.393T=
ENST00000697850.1:n.149T=
ENST00000697851.1:n.393T=
ENST00000638186.1:n.223T=
ENST00000638360.1:n.157T=
ENST00000638925.1:n.156T=
ENST00000650539.1:n.325T=
ENST00000330775.9:c.-81T=	ENSP00000476242.2:n.-81T=
ENST00000357590.9:c.-81T=	ENSP00000476176.2:n.-81T=
ENST00000525039.5:n.343T=
ENST00000525102.5:n.677T=
ENST00000525787.1:n.215T=
ENST00000526626.6:n.115T=
ENST00000527992.5:n.147T=
ENST00000530407.5:n.139T=
ENST00000532085.1:n.1414T=
ENST00000532888.6:n.115T=
ENST00000534384.1:n.140T=
ENST00000538950.5:c.-230T=	ENSP00000475991.2:n.-230T=
ENST00000545985.5:c.-81T=	ENSP00000475241.2:n.-81T=
NM_001164277.1:c.-81T= , LRG_187t1:c.-81T=	NP_001157749.1:n.-81T=
NM_001164278.1:c.-81T=	NP_001157750.1:n.-81T=
NM_001164279.1:c.-230T=	NP_001157751.1:n.-230T=
NM_001164280.1:c.-81T=	NP_001157752.1:n.-81T=
NM_001467.5:c.-81T=	NP_001458.1:n.-81T=
NM_001164278.2:c.-81T=	NP_001157750.1:n.-81T=
NM_001164279.2:c.-230T=	NP_001157751.1:n.-230T=
NM_001164280.2:c.-81T=	NP_001157752.1:n.-81T=
NM_001467.6:c.-81T=	NP_001458.1:n.-81T=
NM_001164277.2:c.-81T= MANE Select	NP_001157749.1:n.-81T=