Canonical Allele Identifier: CA387235525

Gene: SLC15A4

Linked Data

• MyVariant Identifiers: chr12:g.129299569A>T (hg19) ; chr12:g.128815024A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128815024A>T , CM000674.2:g.128815024A>T	GRCh38
NC_000012.11:g.129299569A>T , CM000674.1:g.129299569A>T	GRCh37
NC_000012.10:g.127865522A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266771.10:c.593T>A MANE Select	ENSP00000266771.5:p.Phe198Tyr
ENST00000266771.9:c.593T>A	ENSP00000266771.5:p.Phe198Tyr
ENST00000366292.6:n.905T>A
ENST00000376740.8:c.172T>A
ENST00000376744.8:c.429T>A
ENST00000535272.1:n.387T>A
ENST00000539703.1:n.243T>A
NM_145648.3:c.593T>A	NP_663623.1:p.Phe198Tyr
XM_011537895.1:c.743T>A	XP_011536197.1:p.Phe248Tyr
XR_429081.2:n.616T>A
XR_944494.1:n.766T>A
XR_944495.1:n.766T>A
XR_944496.1:n.766T>A
XR_944497.1:n.766T>A
XM_017018791.1:c.743T>A	XP_016874280.1:p.Phe248Tyr
XM_017018792.1:c.743T>A	XP_016874281.1:p.Phe248Tyr
XM_017018793.1:c.593T>A	XP_016874282.1:p.Phe198Tyr
XR_002957287.1:n.616T>A
XR_944496.2:n.766T>A
NM_145648.4:c.593T>A MANE Select	NP_663623.1:p.Phe198Tyr