Canonical Allele Identifier: CA2003749713

Gene: SLC37A4

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027741T= , CM000673.2:g.119027741T=	GRCh38
NC_000011.9:g.118898451T= , CM000673.1:g.118898451T=	GRCh37
NC_000011.8:g.118403661T=	NCBI36
NG_013331.1:g.8166A= , LRG_187:g.8166A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.742A=
ENST00000697845.1:n.666A=
ENST00000697846.1:n.742A=
ENST00000697847.1:n.742A=
ENST00000697848.1:n.742A=
ENST00000697849.1:n.1781A=
ENST00000697850.1:n.742A=
ENST00000697851.1:n.2102A=
ENST00000638186.1:n.816A=
ENST00000638360.1:n.648A=
ENST00000638925.1:n.749A=
ENST00000650539.1:n.918A=
ENST00000330775.9:c.513A=	ENSP00000476242.2:p.Leu171=
ENST00000357590.9:c.513A=	ENSP00000476176.2:p.Leu171=
ENST00000524428.5:n.834A=
ENST00000525039.5:n.936A=
ENST00000525102.5:n.1270A=
ENST00000525372.5:n.513A=
ENST00000526275.5:n.1294A=
ENST00000526626.6:n.475A=
ENST00000527992.5:n.740A=
ENST00000529510.5:n.399+453A=
ENST00000530407.5:n.662A=
ENST00000532085.1:n.3123A=
ENST00000532888.6:n.808A=
ENST00000538950.5:c.294A=	ENSP00000475991.2:p.Leu98=
ENST00000545985.5:c.513A=	ENSP00000475241.2:p.Leu171=
NM_001164277.1:c.513A= , LRG_187t1:c.513A=	NP_001157749.1:p.Leu171=
NM_001164278.1:c.513A=	NP_001157750.1:p.Leu171=
NM_001164279.1:c.294A=	NP_001157751.1:p.Leu98=
NM_001164280.1:c.513A=	NP_001157752.1:p.Leu171=
NM_001467.5:c.513A=	NP_001458.1:p.Leu171=
NM_001164278.2:c.513A=	NP_001157750.1:p.Leu171=
NM_001164279.2:c.294A=	NP_001157751.1:p.Leu98=
NM_001164280.2:c.513A=	NP_001157752.1:p.Leu171=
NM_001467.6:c.513A=	NP_001458.1:p.Leu171=
NM_001164277.2:c.513A= MANE Select	NP_001157749.1:p.Leu171=