Canonical Allele Identifier: CA2616334504

Gene: SLC37A4

Linked Data

• gnomAD v4: 11-119026309-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026309A>G , CM000673.2:g.119026309A>G	GRCh38
NC_000011.9:g.118897019A>G , CM000673.1:g.118897019A>G	GRCh37
NC_000011.8:g.118402229A>G	NCBI36
NG_013331.1:g.9597T>C , LRG_187:g.9597T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1015-229T>C
ENST00000697845.1:n.1566T>C
ENST00000697846.1:n.1015-229T>C
ENST00000697847.1:n.1201+193T>C
ENST00000697848.1:n.1101-229T>C
ENST00000697849.1:n.2681T>C
ENST00000697850.1:n.1101-229T>C
ENST00000697851.1:n.2709-229T>C
ENST00000638186.1:n.1175-229T>C
ENST00000638360.1:n.1007-229T>C
ENST00000638925.1:n.1140-229T>C
ENST00000650539.1:n.1277-229T>C
ENST00000330775.9:c.871-229T>C	ENSP00000476242.2:n.871-229T>C
ENST00000357590.9:c.871-229T>C	ENSP00000476176.2:n.871-229T>C
ENST00000524428.5:n.1107-229T>C
ENST00000525039.5:n.1295-229T>C
ENST00000525102.5:n.1629-229T>C
ENST00000525372.5:n.968+197T>C
ENST00000526275.5:n.1653-229T>C
ENST00000527992.5:n.1099-229T>C
ENST00000529510.5:n.559-229T>C
ENST00000530407.5:n.1021-229T>C
ENST00000532085.1:n.4023T>C
ENST00000538950.5:c.652-229T>C	ENSP00000475991.2:n.652-229T>C
ENST00000545985.5:c.871-229T>C	ENSP00000475241.2:n.871-229T>C
NM_001164277.1:c.871-229T>C , LRG_187t1:c.871-229T>C	NP_001157749.1:n.871-229T>C
NM_001164278.1:c.871-229T>C	NP_001157750.1:n.871-229T>C
NM_001164279.1:c.652-229T>C	NP_001157751.1:n.652-229T>C
NM_001164280.1:c.871-229T>C	NP_001157752.1:n.871-229T>C
NM_001467.5:c.871-229T>C	NP_001458.1:n.871-229T>C
NM_001164278.2:c.871-229T>C	NP_001157750.1:n.871-229T>C
NM_001164279.2:c.652-229T>C	NP_001157751.1:n.652-229T>C
NM_001164280.2:c.871-229T>C	NP_001157752.1:n.871-229T>C
NM_001467.6:c.871-229T>C	NP_001458.1:n.871-229T>C
NM_001164277.2:c.871-229T>C MANE Select	NP_001157749.1:n.871-229T>C