Canonical Allele Identifier: CA382897097

Gene: SLC37A4

Linked Data

• gnomAD v4: 11-119025968-T-A
• MyVariant Identifiers: chr11:g.118896678T>A (hg19) ; chr11:g.119025968T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119025968T>A , CM000673.2:g.119025968T>A	GRCh38
NC_000011.9:g.118896678T>A , CM000673.1:g.118896678T>A	GRCh37
NC_000011.8:g.118401888T>A	NCBI36
NG_013331.1:g.9938A>T , LRG_187:g.9938A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.1127A>T
ENST00000697845.1:n.1907A>T
ENST00000697846.1:n.1127A>T
ENST00000697847.1:n.1202-211A>T
ENST00000697848.1:n.1213A>T
ENST00000697849.1:n.3022A>T
ENST00000697850.1:n.1213A>T
ENST00000697851.1:n.2821A>T
ENST00000638186.1:n.1287A>T
ENST00000638360.1:n.1119A>T
ENST00000638925.1:n.1252A>T
ENST00000650539.1:n.1389A>T
ENST00000330775.9:c.983A>T	ENSP00000476242.2:p.Lys328Met
ENST00000357590.9:c.983A>T	ENSP00000476176.2:p.Lys328Met
ENST00000524428.5:n.1219A>T
ENST00000525039.5:n.1407A>T
ENST00000525102.5:n.1741A>T
ENST00000525372.5:n.1081A>T
ENST00000526275.5:n.1765A>T
ENST00000527992.5:n.1211A>T
ENST00000529510.5:n.671A>T
ENST00000530407.5:n.1133A>T
ENST00000532085.1:n.4364A>T
ENST00000538950.5:c.764A>T	ENSP00000475991.2:p.Lys255Met
ENST00000545985.5:c.983A>T	ENSP00000475241.2:p.Lys328Met
NM_001164277.1:c.983A>T , LRG_187t1:c.983A>T	NP_001157749.1:p.Lys328Met
NM_001164278.1:c.983A>T	NP_001157750.1:p.Lys328Met
NM_001164279.1:c.764A>T	NP_001157751.1:p.Lys255Met
NM_001164280.1:c.983A>T	NP_001157752.1:p.Lys328Met
NM_001467.5:c.983A>T	NP_001458.1:p.Lys328Met
NM_001164278.2:c.983A>T	NP_001157750.1:p.Lys328Met
NM_001164279.2:c.764A>T	NP_001157751.1:p.Lys255Met
NM_001164280.2:c.983A>T	NP_001157752.1:p.Lys328Met
NM_001467.6:c.983A>T	NP_001458.1:p.Lys328Met
NM_001164277.2:c.983A>T MANE Select	NP_001157749.1:p.Lys328Met