Canonical Allele Identifier: CA387234974

Gene: SLC15A4

Linked Data

• MyVariant Identifiers: chr12:g.129299387C>A (hg19) ; chr12:g.128814842C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128814842C>A , CM000674.2:g.128814842C>A	GRCh38
NC_000012.11:g.129299387C>A , CM000674.1:g.129299387C>A	GRCh37
NC_000012.10:g.127865340C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266771.10:c.775G>T MANE Select	ENSP00000266771.5:p.Asp259Tyr
ENST00000266771.9:c.775G>T	ENSP00000266771.5:p.Asp259Tyr
ENST00000366292.6:n.1087G>T
ENST00000376740.8:c.354G>T
ENST00000376744.8:c.611G>T
ENST00000539703.1:n.425G>T
ENST00000614634.1:c.-68G>T	ENSP00000483143.1:n.-68G>T
NM_145648.3:c.775G>T	NP_663623.1:p.Asp259Tyr
XM_011537895.1:c.925G>T	XP_011536197.1:p.Asp309Tyr
XR_429081.2:n.798G>T
XR_944494.1:n.948G>T
XR_944495.1:n.948G>T
XR_944496.1:n.948G>T
XR_944497.1:n.948G>T
XM_017018791.1:c.925G>T	XP_016874280.1:p.Asp309Tyr
XM_017018792.1:c.925G>T	XP_016874281.1:p.Asp309Tyr
XM_017018793.1:c.775G>T	XP_016874282.1:p.Asp259Tyr
XR_002957287.1:n.798G>T
XR_944496.2:n.948G>T
NM_145648.4:c.775G>T MANE Select	NP_663623.1:p.Asp259Tyr