Canonical Allele Identifier: CA387234681

Gene: SLC15A4

Linked Data

• MyVariant Identifiers: chr12:g.129299321C>G (hg19) ; chr12:g.128814776C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128814776C>G , CM000674.2:g.128814776C>G	GRCh38
NC_000012.11:g.129299321C>G , CM000674.1:g.129299321C>G	GRCh37
NC_000012.10:g.127865274C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000266771.10:c.841G>C MANE Select	ENSP00000266771.5:p.Gly281Arg
ENST00000266771.9:c.841G>C	ENSP00000266771.5:p.Gly281Arg
ENST00000366292.6:n.1153G>C
ENST00000376740.8:c.420G>C
ENST00000376744.8:c.677G>C
ENST00000539703.1:n.491G>C
ENST00000614634.1:c.-2G>C	ENSP00000483143.1:n.-2G>C
NM_145648.3:c.841G>C	NP_663623.1:p.Gly281Arg
XM_011537895.1:c.991G>C	XP_011536197.1:p.Gly331Arg
XR_429081.2:n.864G>C
XR_944494.1:n.1014G>C
XR_944495.1:n.1014G>C
XR_944496.1:n.1014G>C
XR_944497.1:n.1014G>C
XM_017018791.1:c.991G>C	XP_016874280.1:p.Gly331Arg
XM_017018792.1:c.991G>C	XP_016874281.1:p.Gly331Arg
XM_017018793.1:c.841G>C	XP_016874282.1:p.Gly281Arg
XR_002957287.1:n.864G>C
XR_944496.2:n.1014G>C
NM_145648.4:c.841G>C MANE Select	NP_663623.1:p.Gly281Arg