Canonical Allele Identifier: CA482620781

Gene: SLC15A4

Linked Data

• MyVariant Identifiers: chr12:g.129299367C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128814822C>G , CM000674.2:g.128814822C>G	GRCh38
NC_000012.11:g.129299367C>G , CM000674.1:g.129299367C>G	GRCh37
NC_000012.10:g.127865320C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266771.10:c.795G>C MANE Select	ENSP00000266771.5:p.Thr265=
ENST00000266771.9:c.795G>C	ENSP00000266771.5:p.Thr265=
ENST00000366292.6:n.1107G>C
ENST00000376740.8:c.374G>C
ENST00000376744.8:c.631G>C
ENST00000539703.1:n.445G>C
ENST00000614634.1:c.-48G>C	ENSP00000483143.1:n.-48G>C
NM_145648.3:c.795G>C	NP_663623.1:p.Thr265=
XM_011537895.1:c.945G>C	XP_011536197.1:p.Thr315=
XR_429081.2:n.818G>C
XR_944494.1:n.968G>C
XR_944495.1:n.968G>C
XR_944496.1:n.968G>C
XR_944497.1:n.968G>C
XM_017018791.1:c.945G>C	XP_016874280.1:p.Thr315=
XM_017018792.1:c.945G>C	XP_016874281.1:p.Thr315=
XM_017018793.1:c.795G>C	XP_016874282.1:p.Thr265=
XR_002957287.1:n.818G>C
XR_944496.2:n.968G>C
NM_145648.4:c.795G>C MANE Select	NP_663623.1:p.Thr265=