Canonical Allele Identifier: CA2616334972

Gene: SLC37A4

Linked Data

• gnomAD v4: 11-119026851-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026851G>T , CM000673.2:g.119026851G>T	GRCh38
NC_000011.9:g.118897561G>T , CM000673.1:g.118897561G>T	GRCh37
NC_000011.8:g.118402771G>T	NCBI36
NG_013331.1:g.9055C>A , LRG_187:g.9055C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1014+86C>A
ENST00000697845.1:n.1024C>A
ENST00000697846.1:n.1014+86C>A
ENST00000697847.1:n.1014+86C>A
ENST00000697848.1:n.1014+86C>A
ENST00000697849.1:n.2139C>A
ENST00000697850.1:n.1014+86C>A
ENST00000697851.1:n.2460C>A
ENST00000638186.1:n.1088+86C>A
ENST00000638360.1:n.920+86C>A
ENST00000638925.1:n.1021+86C>A
ENST00000650539.1:n.1190+86C>A
ENST00000330775.9:c.784+86C>A	ENSP00000476242.2:n.784+86C>A
ENST00000357590.9:c.784+86C>A	ENSP00000476176.2:n.784+86C>A
ENST00000524428.5:n.1106+86C>A
ENST00000525039.5:n.1208+86C>A
ENST00000525102.5:n.1542+86C>A
ENST00000525372.5:n.785+86C>A
ENST00000526275.5:n.1566+86C>A
ENST00000527992.5:n.1012+86C>A
ENST00000529510.5:n.558+86C>A
ENST00000530407.5:n.934+86C>A
ENST00000532085.1:n.3481C>A
ENST00000532888.6:n.1166C>A
ENST00000538950.5:c.565+86C>A	ENSP00000475991.2:n.565+86C>A
ENST00000545985.5:c.784+86C>A	ENSP00000475241.2:n.784+86C>A
NM_001164277.1:c.784+86C>A , LRG_187t1:c.784+86C>A	NP_001157749.1:n.784+86C>A
NM_001164278.1:c.784+86C>A	NP_001157750.1:n.784+86C>A
NM_001164279.1:c.565+86C>A	NP_001157751.1:n.565+86C>A
NM_001164280.1:c.784+86C>A	NP_001157752.1:n.784+86C>A
NM_001467.5:c.784+86C>A	NP_001458.1:n.784+86C>A
NM_001164278.2:c.784+86C>A	NP_001157750.1:n.784+86C>A
NM_001164279.2:c.565+86C>A	NP_001157751.1:n.565+86C>A
NM_001164280.2:c.784+86C>A	NP_001157752.1:n.784+86C>A
NM_001467.6:c.784+86C>A	NP_001458.1:n.784+86C>A
NM_001164277.2:c.784+86C>A MANE Select	NP_001157749.1:n.784+86C>A