Canonical Allele Identifier: CA6311697

Gene: SLC37A4

Linked Data

• ClinVar Variation Id: 557737
• ClinVar RCV Id: RCV000673914
• dbSNP Id: rs781985446
• ExAC: 11:118896796 G / C
• gnomAD v2: 11-118896796-G-C
• gnomAD v3: 11-119026086-G-C
• gnomAD v4: 11-119026086-G-C
• MyVariant Identifiers: chr11:g.118896796G>C (hg19) ; chr11:g.119026086G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026086G>C , CM000673.2:g.119026086G>C	GRCh38
NC_000011.9:g.118896796G>C , CM000673.1:g.118896796G>C	GRCh37
NC_000011.8:g.118402006G>C	NCBI36
NG_013331.1:g.9820C>G , LRG_187:g.9820C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1015-6C>G
ENST00000697845.1:n.1789C>G
ENST00000697846.1:n.1015-6C>G
ENST00000697847.1:n.1202-329C>G
ENST00000697848.1:n.1101-6C>G
ENST00000697849.1:n.2904C>G
ENST00000697850.1:n.1101-6C>G
ENST00000697851.1:n.2709-6C>G
ENST00000638186.1:n.1175-6C>G
ENST00000638360.1:n.1007-6C>G
ENST00000638925.1:n.1140-6C>G
ENST00000650539.1:n.1277-6C>G
ENST00000330775.9:c.871-6C>G	ENSP00000476242.2:n.871-6C>G
ENST00000357590.9:c.871-6C>G	ENSP00000476176.2:n.871-6C>G
ENST00000524428.5:n.1107-6C>G
ENST00000525039.5:n.1295-6C>G
ENST00000525102.5:n.1629-6C>G
ENST00000525372.5:n.969-6C>G
ENST00000526275.5:n.1653-6C>G
ENST00000527992.5:n.1099-6C>G
ENST00000529510.5:n.559-6C>G
ENST00000530407.5:n.1021-6C>G
ENST00000532085.1:n.4246C>G
ENST00000538950.5:c.652-6C>G	ENSP00000475991.2:n.652-6C>G
ENST00000545985.5:c.871-6C>G	ENSP00000475241.2:n.871-6C>G
NM_001164277.1:c.871-6C>G , LRG_187t1:c.871-6C>G	NP_001157749.1:n.871-6C>G
NM_001164278.1:c.871-6C>G	NP_001157750.1:n.871-6C>G
NM_001164279.1:c.652-6C>G	NP_001157751.1:n.652-6C>G
NM_001164280.1:c.871-6C>G	NP_001157752.1:n.871-6C>G
NM_001467.5:c.871-6C>G	NP_001458.1:n.871-6C>G
NM_001164278.2:c.871-6C>G	NP_001157750.1:n.871-6C>G
NM_001164279.2:c.652-6C>G	NP_001157751.1:n.652-6C>G
NM_001164280.2:c.871-6C>G	NP_001157752.1:n.871-6C>G
NM_001467.6:c.871-6C>G	NP_001458.1:n.871-6C>G
NM_001164277.2:c.871-6C>G MANE Select	NP_001157749.1:n.871-6C>G