Canonical Allele Identifier: CA382898058

Gene: SLC37A4

Linked Data

• gnomAD v4: 11-119026061-C-A
• MyVariant Identifiers: chr11:g.118896771C>A (hg19) ; chr11:g.119026061C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119026061C>A , CM000673.2:g.119026061C>A	GRCh38
NC_000011.9:g.118896771C>A , CM000673.1:g.118896771C>A	GRCh37
NC_000011.8:g.118401981C>A	NCBI36
NG_013331.1:g.9845G>T , LRG_187:g.9845G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1034G>T
ENST00000697845.1:n.1814G>T
ENST00000697846.1:n.1034G>T
ENST00000697847.1:n.1202-304G>T
ENST00000697848.1:n.1120G>T
ENST00000697849.1:n.2929G>T
ENST00000697850.1:n.1120G>T
ENST00000697851.1:n.2728G>T
ENST00000638186.1:n.1194G>T
ENST00000638360.1:n.1026G>T
ENST00000638925.1:n.1159G>T
ENST00000650539.1:n.1296G>T
ENST00000330775.9:c.890G>T	ENSP00000476242.2:p.Gly297Val
ENST00000357590.9:c.890G>T	ENSP00000476176.2:p.Gly297Val
ENST00000524428.5:n.1126G>T
ENST00000525039.5:n.1314G>T
ENST00000525102.5:n.1648G>T
ENST00000525372.5:n.988G>T
ENST00000526275.5:n.1672G>T
ENST00000527992.5:n.1118G>T
ENST00000529510.5:n.578G>T
ENST00000530407.5:n.1040G>T
ENST00000532085.1:n.4271G>T
ENST00000538950.5:c.671G>T	ENSP00000475991.2:p.Gly224Val
ENST00000545985.5:c.890G>T	ENSP00000475241.2:p.Gly297Val
NM_001164277.1:c.890G>T , LRG_187t1:c.890G>T	NP_001157749.1:p.Gly297Val
NM_001164278.1:c.890G>T	NP_001157750.1:p.Gly297Val
NM_001164279.1:c.671G>T	NP_001157751.1:p.Gly224Val
NM_001164280.1:c.890G>T	NP_001157752.1:p.Gly297Val
NM_001467.5:c.890G>T	NP_001458.1:p.Gly297Val
NM_001164278.2:c.890G>T	NP_001157750.1:p.Gly297Val
NM_001164279.2:c.671G>T	NP_001157751.1:p.Gly224Val
NM_001164280.2:c.890G>T	NP_001157752.1:p.Gly297Val
NM_001467.6:c.890G>T	NP_001458.1:p.Gly297Val
NM_001164277.2:c.890G>T MANE Select	NP_001157749.1:p.Gly297Val