Canonical Allele Identifier: CA672376626

Gene: SLC37A4

Linked Data

• dbSNP Id: rs1420686539
• gnomAD v3: 11-119026543-C-G
• gnomAD v4: 11-119026543-C-G
• MyVariant Identifiers: chr11:g.118897253C>G (hg19) ; chr11:g.119026543C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026543C>G , CM000673.2:g.119026543C>G	GRCh38
NC_000011.9:g.118897253C>G , CM000673.1:g.118897253C>G	GRCh37
NC_000011.8:g.118402463C>G	NCBI36
NG_013331.1:g.9363G>C , LRG_187:g.9363G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000529510.6:n.1014+394G>C
ENST00000697845.1:n.1332G>C
ENST00000697846.1:n.1014+394G>C
ENST00000697847.1:n.1160G>C
ENST00000697848.1:n.1100+60G>C
ENST00000697849.1:n.2447G>C
ENST00000697850.1:n.1100+60G>C
ENST00000697851.1:n.2708+60G>C
ENST00000638186.1:n.1174+60G>C
ENST00000638360.1:n.1006+60G>C
ENST00000638925.1:n.1139+28G>C
ENST00000650539.1:n.1276+60G>C
ENST00000330775.9:c.870+60G>C	ENSP00000476242.2:n.870+60G>C
ENST00000357590.9:c.870+60G>C	ENSP00000476176.2:n.870+60G>C
ENST00000524428.5:n.1106+394G>C
ENST00000525039.5:n.1294+60G>C
ENST00000525102.5:n.1628+60G>C
ENST00000525372.5:n.931G>C
ENST00000526275.5:n.1652+60G>C
ENST00000527992.5:n.1098+60G>C
ENST00000529510.5:n.558+394G>C
ENST00000530407.5:n.1020+60G>C
ENST00000532085.1:n.3789G>C
ENST00000538950.5:c.651+60G>C	ENSP00000475991.2:n.651+60G>C
ENST00000545985.5:c.870+60G>C	ENSP00000475241.2:n.870+60G>C
NM_001164277.1:c.870+60G>C , LRG_187t1:c.870+60G>C	NP_001157749.1:n.870+60G>C
NM_001164278.1:c.870+60G>C	NP_001157750.1:n.870+60G>C
NM_001164279.1:c.651+60G>C	NP_001157751.1:n.651+60G>C
NM_001164280.1:c.870+60G>C	NP_001157752.1:n.870+60G>C
NM_001467.5:c.870+60G>C	NP_001458.1:n.870+60G>C
NM_001164278.2:c.870+60G>C	NP_001157750.1:n.870+60G>C
NM_001164279.2:c.651+60G>C	NP_001157751.1:n.651+60G>C
NM_001164280.2:c.870+60G>C	NP_001157752.1:n.870+60G>C
NM_001467.6:c.870+60G>C	NP_001458.1:n.870+60G>C
NM_001164277.2:c.870+60G>C MANE Select	NP_001157749.1:n.870+60G>C