Canonical Allele Identifier: CA387235349

Gene: SLC15A4

Linked Data

• gnomAD v4: 12-128814946-G-A
• MyVariant Identifiers: chr12:g.129299491G>A (hg19) ; chr12:g.128814946G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128814946G>A , CM000674.2:g.128814946G>A	GRCh38
NC_000012.11:g.129299491G>A , CM000674.1:g.129299491G>A	GRCh37
NC_000012.10:g.127865444G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266771.10:c.671C>T MANE Select	ENSP00000266771.5:p.Thr224Ile
ENST00000266771.9:c.671C>T	ENSP00000266771.5:p.Thr224Ile
ENST00000366292.6:n.983C>T
ENST00000376740.8:c.250C>T
ENST00000376744.8:c.507C>T
ENST00000539703.1:n.321C>T
ENST00000614634.1:c.-172C>T	ENSP00000483143.1:n.-172C>T
NM_145648.3:c.671C>T	NP_663623.1:p.Thr224Ile
XM_011537895.1:c.821C>T	XP_011536197.1:p.Thr274Ile
XR_429081.2:n.694C>T
XR_944494.1:n.844C>T
XR_944495.1:n.844C>T
XR_944496.1:n.844C>T
XR_944497.1:n.844C>T
XM_017018791.1:c.821C>T	XP_016874280.1:p.Thr274Ile
XM_017018792.1:c.821C>T	XP_016874281.1:p.Thr274Ile
XM_017018793.1:c.671C>T	XP_016874282.1:p.Thr224Ile
XR_002957287.1:n.694C>T
XR_944496.2:n.844C>T
NM_145648.4:c.671C>T MANE Select	NP_663623.1:p.Thr224Ile