Canonical Allele Identifier: CA4514056

Gene: SLC37A3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140369628C>T , CM000669.2:g.140369628C>T	GRCh38
NC_000007.13:g.140069428C>T , CM000669.1:g.140069428C>T	GRCh37
NC_000007.12:g.139715897C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_207113.3:c.253G>A MANE Select	NP_996996.1:p.Gly85Ser
ENST00000326232.14:c.253G>A MANE Select	ENSP00000321498.9:p.Gly85Ser
NM_001287498.1:c.253G>A	NP_001274427.1:p.Gly85Ser
NM_001287498.2:c.253G>A	NP_001274427.1:p.Gly85Ser
NM_001363373.1:c.253G>A	NP_001350302.1:p.Gly85Ser
NM_001363374.1:c.253G>A	NP_001350303.1:p.Gly85Ser
NM_001363375.1:c.253G>A	NP_001350304.1:p.Gly85Ser
NM_001363376.1:c.253G>A	NP_001350305.1:p.Gly85Ser
NM_001363377.1:c.253G>A	NP_001350306.1:p.Gly85Ser
NM_001363378.1:c.253G>A	NP_001350307.1:p.Gly85Ser
NM_032295.3:c.253G>A	NP_115671.1:p.Gly85Ser
NM_032295.4:c.253G>A	NP_115671.1:p.Gly85Ser
NM_207113.2:c.253G>A	NP_996996.1:p.Gly85Ser
NR_156489.1:n.438G>A
NR_156490.1:n.438G>A
NR_156491.1:n.438G>A
NR_156492.1:n.438G>A
ENST00000326232.13:c.253G>A	ENSP00000321498.9:p.Gly85Ser
ENST00000340308.7:c.253G>A	ENSP00000343358.3:p.Gly85Ser
ENST00000447932.6:c.253G>A	ENSP00000397481.2:p.Gly85Ser
ENST00000460560.5:n.416G>A
ENST00000461089.5:n.349G>A
ENST00000462881.1:c.*146G>A	ENSP00000419410.1:n.*146G>A
ENST00000464834.5:c.35G>A
ENST00000464865.5:n.412G>A
ENST00000469193.5:c.253G>A	ENSP00000419024.1:p.Gly85Ser
ENST00000473707.5:n.55G>A
ENST00000477571.5:c.253G>A	ENSP00000417365.1:p.Gly85Ser
ENST00000485861.5:c.27G>A
ENST00000490760.5:c.90-10843G>A	ENSP00000418585.1:n.90-10843G>A
XM_011516626.1:c.253G>A	XP_011514928.1:p.Gly85Ser
XM_011516627.1:c.253G>A	XP_011514929.1:p.Gly85Ser
XR_927543.1:n.547G>A