Canonical Allele Identifier: CA229600365

Gene: SLC37A4

Linked Data

• dbSNP Id: rs961721941
• gnomAD v2: 11-118899490-C-T
• gnomAD v3: 11-119028780-C-T
• gnomAD v4: 11-119028780-C-T
• MyVariant Identifiers: chr11:g.118899490C>T (hg19) ; chr11:g.119028780C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119028780C>T , CM000673.2:g.119028780C>T	GRCh38
NC_000011.9:g.118899490C>T , CM000673.1:g.118899490C>T	GRCh37
NC_000011.8:g.118404700C>T	NCBI36
NG_013331.1:g.7127G>A , LRG_187:g.7127G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.378-354G>A
ENST00000697846.1:n.378-354G>A
ENST00000697847.1:n.378-354G>A
ENST00000697848.1:n.378-354G>A
ENST00000697849.1:n.1063G>A
ENST00000697850.1:n.378-354G>A
ENST00000697851.1:n.1063G>A
ENST00000638186.1:n.452-354G>A
ENST00000638360.1:n.386-354G>A
ENST00000638925.1:n.385-354G>A
ENST00000650539.1:n.554-354G>A
ENST00000330775.9:c.149-354G>A	ENSP00000476242.2:n.149-354G>A
ENST00000357590.9:c.149-354G>A	ENSP00000476176.2:n.149-354G>A
ENST00000524428.5:n.149-354G>A
ENST00000525039.5:n.572-354G>A
ENST00000525102.5:n.906-354G>A
ENST00000525372.5:n.149-354G>A
ENST00000525787.1:n.444-354G>A
ENST00000526275.5:n.255G>A
ENST00000526626.6:n.343+442G>A
ENST00000527992.5:n.376-354G>A
ENST00000529510.5:n.167-354G>A
ENST00000530407.5:n.252G>A
ENST00000532085.1:n.2084G>A
ENST00000532888.6:n.398G>A
ENST00000534384.1:n.369-354G>A
ENST00000538950.5:c.-117G>A	ENSP00000475991.2:n.-117G>A
ENST00000545985.5:c.149-354G>A	ENSP00000475241.2:n.149-354G>A
NM_001164277.1:c.149-354G>A , LRG_187t1:c.149-354G>A	NP_001157749.1:n.149-354G>A
NM_001164278.1:c.149-354G>A	NP_001157750.1:n.149-354G>A
NM_001164279.1:c.-117G>A	NP_001157751.1:n.-117G>A
NM_001164280.1:c.149-354G>A	NP_001157752.1:n.149-354G>A
NM_001467.5:c.149-354G>A	NP_001458.1:n.149-354G>A
NM_001164278.2:c.149-354G>A	NP_001157750.1:n.149-354G>A
NM_001164279.2:c.-117G>A	NP_001157751.1:n.-117G>A
NM_001164280.2:c.149-354G>A	NP_001157752.1:n.149-354G>A
NM_001467.6:c.149-354G>A	NP_001458.1:n.149-354G>A
NM_001164277.2:c.149-354G>A MANE Select	NP_001157749.1:n.149-354G>A