Canonical Allele Identifier: CA382903569

Gene: SLC37A4

Linked Data

• MyVariant Identifiers: chr11:g.118898527T>A (hg19) ; chr11:g.119027817T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027817T>A , CM000673.2:g.119027817T>A	GRCh38
NC_000011.9:g.118898527T>A , CM000673.1:g.118898527T>A	GRCh37
NC_000011.8:g.118403737T>A	NCBI36
NG_013331.1:g.8090A>T , LRG_187:g.8090A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.666A>T
ENST00000697845.1:n.590A>T
ENST00000697846.1:n.666A>T
ENST00000697847.1:n.666A>T
ENST00000697848.1:n.666A>T
ENST00000697849.1:n.1705A>T
ENST00000697850.1:n.666A>T
ENST00000697851.1:n.2026A>T
ENST00000638186.1:n.740A>T
ENST00000638360.1:n.619-47A>T
ENST00000638925.1:n.673A>T
ENST00000650539.1:n.842A>T
ENST00000330775.9:c.437A>T	ENSP00000476242.2:p.Asn146Ile
ENST00000357590.9:c.437A>T	ENSP00000476176.2:p.Asn146Ile
ENST00000524428.5:n.758A>T
ENST00000525039.5:n.860A>T
ENST00000525102.5:n.1194A>T
ENST00000525372.5:n.437A>T
ENST00000525787.1:n.1053A>T
ENST00000526275.5:n.1218A>T
ENST00000526626.6:n.399A>T
ENST00000527992.5:n.664A>T
ENST00000529510.5:n.399+377A>T
ENST00000530407.5:n.586A>T
ENST00000532085.1:n.3047A>T
ENST00000532888.6:n.732A>T
ENST00000538950.5:c.218A>T	ENSP00000475991.2:p.Asn73Ile
ENST00000545985.5:c.437A>T	ENSP00000475241.2:p.Asn146Ile
NM_001164277.1:c.437A>T , LRG_187t1:c.437A>T	NP_001157749.1:p.Asn146Ile
NM_001164278.1:c.437A>T	NP_001157750.1:p.Asn146Ile
NM_001164279.1:c.218A>T	NP_001157751.1:p.Asn73Ile
NM_001164280.1:c.437A>T	NP_001157752.1:p.Asn146Ile
NM_001467.5:c.437A>T	NP_001458.1:p.Asn146Ile
NM_001164278.2:c.437A>T	NP_001157750.1:p.Asn146Ile
NM_001164279.2:c.218A>T	NP_001157751.1:p.Asn73Ile
NM_001164280.2:c.437A>T	NP_001157752.1:p.Asn146Ile
NM_001467.6:c.437A>T	NP_001458.1:p.Asn146Ile
NM_001164277.2:c.437A>T MANE Select	NP_001157749.1:p.Asn146Ile