Canonical Allele Identifier: CA2616337088

Gene: SLC37A4

Linked Data

• gnomAD v4: 11-119028758-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119028758G>T , CM000673.2:g.119028758G>T	GRCh38
NC_000011.9:g.118899468G>T , CM000673.1:g.118899468G>T	GRCh37
NC_000011.8:g.118404678G>T	NCBI36
NG_013331.1:g.7149C>A , LRG_187:g.7149C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.378-332C>A
ENST00000697846.1:n.378-332C>A
ENST00000697847.1:n.378-332C>A
ENST00000697848.1:n.378-332C>A
ENST00000697849.1:n.1085C>A
ENST00000697850.1:n.378-332C>A
ENST00000697851.1:n.1085C>A
ENST00000638186.1:n.452-332C>A
ENST00000638360.1:n.386-332C>A
ENST00000638925.1:n.385-332C>A
ENST00000650539.1:n.554-332C>A
ENST00000330775.9:c.149-332C>A	ENSP00000476242.2:n.149-332C>A
ENST00000357590.9:c.149-332C>A	ENSP00000476176.2:n.149-332C>A
ENST00000524428.5:n.149-332C>A
ENST00000525039.5:n.572-332C>A
ENST00000525102.5:n.906-332C>A
ENST00000525372.5:n.149-332C>A
ENST00000525787.1:n.444-332C>A
ENST00000526275.5:n.277C>A
ENST00000526626.6:n.343+464C>A
ENST00000527992.5:n.376-332C>A
ENST00000529510.5:n.167-332C>A
ENST00000530407.5:n.274C>A
ENST00000532085.1:n.2106C>A
ENST00000532888.6:n.420C>A
ENST00000534384.1:n.369-332C>A
ENST00000538950.5:c.-95C>A	ENSP00000475991.2:n.-95C>A
ENST00000545985.5:c.149-332C>A	ENSP00000475241.2:n.149-332C>A
NM_001164277.1:c.149-332C>A , LRG_187t1:c.149-332C>A	NP_001157749.1:n.149-332C>A
NM_001164278.1:c.149-332C>A	NP_001157750.1:n.149-332C>A
NM_001164279.1:c.-95C>A	NP_001157751.1:n.-95C>A
NM_001164280.1:c.149-332C>A	NP_001157752.1:n.149-332C>A
NM_001467.5:c.149-332C>A	NP_001458.1:n.149-332C>A
NM_001164278.2:c.149-332C>A	NP_001157750.1:n.149-332C>A
NM_001164279.2:c.-95C>A	NP_001157751.1:n.-95C>A
NM_001164280.2:c.149-332C>A	NP_001157752.1:n.149-332C>A
NM_001467.6:c.149-332C>A	NP_001458.1:n.149-332C>A
NM_001164277.2:c.149-332C>A MANE Select	NP_001157749.1:n.149-332C>A