Canonical Allele Identifier: CA387235526

Gene: SLC15A4

Linked Data

• MyVariant Identifiers: chr12:g.129299570A>C (hg19) ; chr12:g.128815025A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128815025A>C , CM000674.2:g.128815025A>C	GRCh38
NC_000012.11:g.129299570A>C , CM000674.1:g.129299570A>C	GRCh37
NC_000012.10:g.127865523A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266771.10:c.592T>G MANE Select	ENSP00000266771.5:p.Phe198Val
ENST00000266771.9:c.592T>G	ENSP00000266771.5:p.Phe198Val
ENST00000366292.6:n.904T>G
ENST00000376740.8:c.171T>G
ENST00000376744.8:c.428T>G
ENST00000535272.1:n.386T>G
ENST00000539703.1:n.242T>G
NM_145648.3:c.592T>G	NP_663623.1:p.Phe198Val
XM_011537895.1:c.742T>G	XP_011536197.1:p.Phe248Val
XR_429081.2:n.615T>G
XR_944494.1:n.765T>G
XR_944495.1:n.765T>G
XR_944496.1:n.765T>G
XR_944497.1:n.765T>G
XM_017018791.1:c.742T>G	XP_016874280.1:p.Phe248Val
XM_017018792.1:c.742T>G	XP_016874281.1:p.Phe248Val
XM_017018793.1:c.592T>G	XP_016874282.1:p.Phe198Val
XR_002957287.1:n.615T>G
XR_944496.2:n.765T>G
NM_145648.4:c.592T>G MANE Select	NP_663623.1:p.Phe198Val