Canonical Allele Identifier: CA477127926

Gene: SLC37A4

Linked Data

• dbSNP Id: rs782713974
• gnomAD v4: 11-119028404-C-G
• MyVariant Identifiers: chr11:g.118899114C>G (hg19) ; chr11:g.119028404C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119028404C>G , CM000673.2:g.119028404C>G	GRCh38
NC_000011.9:g.118899114C>G , CM000673.1:g.118899114C>G	GRCh37
NC_000011.8:g.118404324C>G	NCBI36
NG_013331.1:g.7503G>C , LRG_187:g.7503G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.400G>C
ENST00000697845.1:n.324G>C
ENST00000697846.1:n.400G>C
ENST00000697847.1:n.400G>C
ENST00000697848.1:n.400G>C
ENST00000697849.1:n.1439G>C
ENST00000697850.1:n.400G>C
ENST00000697851.1:n.1439G>C
ENST00000638186.1:n.474G>C
ENST00000638360.1:n.408G>C
ENST00000638925.1:n.407G>C
ENST00000650539.1:n.576G>C
ENST00000330775.9:c.171G>C	ENSP00000476242.2:p.Ser57=
ENST00000357590.9:c.171G>C	ENSP00000476176.2:p.Ser57=
ENST00000524428.5:n.171G>C
ENST00000525039.5:n.594G>C
ENST00000525102.5:n.928G>C
ENST00000525372.5:n.171G>C
ENST00000525787.1:n.466G>C
ENST00000526275.5:n.631G>C
ENST00000526626.6:n.344-532G>C
ENST00000527992.5:n.398G>C
ENST00000529510.5:n.189G>C
ENST00000530407.5:n.320G>C
ENST00000532085.1:n.2460G>C
ENST00000532888.6:n.466G>C
ENST00000534384.1:n.391G>C
ENST00000538950.5:c.-49G>C	ENSP00000475991.2:n.-49G>C
ENST00000545985.5:c.171G>C	ENSP00000475241.2:p.Ser57=
NM_001164277.1:c.171G>C , LRG_187t1:c.171G>C	NP_001157749.1:p.Ser57=
NM_001164278.1:c.171G>C	NP_001157750.1:p.Ser57=
NM_001164279.1:c.-49G>C	NP_001157751.1:n.-49G>C
NM_001164280.1:c.171G>C	NP_001157752.1:p.Ser57=
NM_001467.5:c.171G>C	NP_001458.1:p.Ser57=
NM_001164278.2:c.171G>C	NP_001157750.1:p.Ser57=
NM_001164279.2:c.-49G>C	NP_001157751.1:n.-49G>C
NM_001164280.2:c.171G>C	NP_001157752.1:p.Ser57=
NM_001467.6:c.171G>C	NP_001458.1:p.Ser57=
NM_001164277.2:c.171G>C MANE Select	NP_001157749.1:p.Ser57=