Canonical Allele Identifier: CA2616335947

Gene: SLC37A4

Linked Data

• gnomAD v4: 11-119027885-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027885G>T , CM000673.2:g.119027885G>T	GRCh38
NC_000011.9:g.118898595G>T , CM000673.1:g.118898595G>T	GRCh37
NC_000011.8:g.118403805G>T	NCBI36
NG_013331.1:g.8022C>A , LRG_187:g.8022C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.611-13C>A
ENST00000697845.1:n.535-13C>A
ENST00000697846.1:n.611-13C>A
ENST00000697847.1:n.611-13C>A
ENST00000697848.1:n.611-13C>A
ENST00000697849.1:n.1650-13C>A
ENST00000697850.1:n.611-13C>A
ENST00000697851.1:n.1958C>A
ENST00000638186.1:n.685-13C>A
ENST00000638360.1:n.619-115C>A
ENST00000638925.1:n.618-13C>A
ENST00000650539.1:n.787-13C>A
ENST00000330775.9:c.382-13C>A	ENSP00000476242.2:n.382-13C>A
ENST00000357590.9:c.382-13C>A	ENSP00000476176.2:n.382-13C>A
ENST00000524428.5:n.690C>A
ENST00000525039.5:n.805-13C>A
ENST00000525102.5:n.1139-13C>A
ENST00000525372.5:n.382-13C>A
ENST00000525787.1:n.985C>A
ENST00000526275.5:n.1150C>A
ENST00000526626.6:n.344-13C>A
ENST00000527992.5:n.609-13C>A
ENST00000529510.5:n.399+309C>A
ENST00000530407.5:n.531-13C>A
ENST00000532085.1:n.2979C>A
ENST00000532888.6:n.677-13C>A
ENST00000538950.5:c.163-13C>A	ENSP00000475991.2:n.163-13C>A
ENST00000545985.5:c.382-13C>A	ENSP00000475241.2:n.382-13C>A
NM_001164277.1:c.382-13C>A , LRG_187t1:c.382-13C>A	NP_001157749.1:n.382-13C>A
NM_001164278.1:c.382-13C>A	NP_001157750.1:n.382-13C>A
NM_001164279.1:c.163-13C>A	NP_001157751.1:n.163-13C>A
NM_001164280.1:c.382-13C>A	NP_001157752.1:n.382-13C>A
NM_001467.5:c.382-13C>A	NP_001458.1:n.382-13C>A
NM_001164278.2:c.382-13C>A	NP_001157750.1:n.382-13C>A
NM_001164279.2:c.163-13C>A	NP_001157751.1:n.163-13C>A
NM_001164280.2:c.382-13C>A	NP_001157752.1:n.382-13C>A
NM_001467.6:c.382-13C>A	NP_001458.1:n.382-13C>A
NM_001164277.2:c.382-13C>A MANE Select	NP_001157749.1:n.382-13C>A