Canonical Allele Identifier: CA2616334552

Gene: SLC37A4

Linked Data

• gnomAD v4: 11-119026374-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026374A>G , CM000673.2:g.119026374A>G	GRCh38
NC_000011.9:g.118897084A>G , CM000673.1:g.118897084A>G	GRCh37
NC_000011.8:g.118402294A>G	NCBI36
NG_013331.1:g.9532T>C , LRG_187:g.9532T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1015-294T>C
ENST00000697845.1:n.1501T>C
ENST00000697846.1:n.1015-294T>C
ENST00000697847.1:n.1201+128T>C
ENST00000697848.1:n.1100+229T>C
ENST00000697849.1:n.2616T>C
ENST00000697850.1:n.1100+229T>C
ENST00000697851.1:n.2708+229T>C
ENST00000638186.1:n.1174+229T>C
ENST00000638360.1:n.1006+229T>C
ENST00000638925.1:n.1139+197T>C
ENST00000650539.1:n.1276+229T>C
ENST00000330775.9:c.870+229T>C	ENSP00000476242.2:n.870+229T>C
ENST00000357590.9:c.870+229T>C	ENSP00000476176.2:n.870+229T>C
ENST00000524428.5:n.1107-294T>C
ENST00000525039.5:n.1294+229T>C
ENST00000525102.5:n.1628+229T>C
ENST00000525372.5:n.968+132T>C
ENST00000526275.5:n.1652+229T>C
ENST00000527992.5:n.1098+229T>C
ENST00000529510.5:n.559-294T>C
ENST00000530407.5:n.1020+229T>C
ENST00000532085.1:n.3958T>C
ENST00000538950.5:c.651+229T>C	ENSP00000475991.2:n.651+229T>C
ENST00000545985.5:c.870+229T>C	ENSP00000475241.2:n.870+229T>C
NM_001164277.1:c.870+229T>C , LRG_187t1:c.870+229T>C	NP_001157749.1:n.870+229T>C
NM_001164278.1:c.870+229T>C	NP_001157750.1:n.870+229T>C
NM_001164279.1:c.651+229T>C	NP_001157751.1:n.651+229T>C
NM_001164280.1:c.870+229T>C	NP_001157752.1:n.870+229T>C
NM_001467.5:c.870+229T>C	NP_001458.1:n.870+229T>C
NM_001164278.2:c.870+229T>C	NP_001157750.1:n.870+229T>C
NM_001164279.2:c.651+229T>C	NP_001157751.1:n.651+229T>C
NM_001164280.2:c.870+229T>C	NP_001157752.1:n.870+229T>C
NM_001467.6:c.870+229T>C	NP_001458.1:n.870+229T>C
NM_001164277.2:c.870+229T>C MANE Select	NP_001157749.1:n.870+229T>C