Canonical Allele Identifier: CA387235500

Gene: SLC15A4

Linked Data

• gnomAD v4: 12-128815015-C-T
• MyVariant Identifiers: chr12:g.129299560C>T (hg19) ; chr12:g.128815015C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128815015C>T , CM000674.2:g.128815015C>T	GRCh38
NC_000012.11:g.129299560C>T , CM000674.1:g.129299560C>T	GRCh37
NC_000012.10:g.127865513C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266771.10:c.602G>A MANE Select	ENSP00000266771.5:p.Ser201Asn
ENST00000266771.9:c.602G>A	ENSP00000266771.5:p.Ser201Asn
ENST00000366292.6:n.914G>A
ENST00000376740.8:c.181G>A
ENST00000376744.8:c.438G>A
ENST00000535272.1:n.396G>A
ENST00000539703.1:n.252G>A
NM_145648.3:c.602G>A	NP_663623.1:p.Ser201Asn
XM_011537895.1:c.752G>A	XP_011536197.1:p.Ser251Asn
XR_429081.2:n.625G>A
XR_944494.1:n.775G>A
XR_944495.1:n.775G>A
XR_944496.1:n.775G>A
XR_944497.1:n.775G>A
XM_017018791.1:c.752G>A	XP_016874280.1:p.Ser251Asn
XM_017018792.1:c.752G>A	XP_016874281.1:p.Ser251Asn
XM_017018793.1:c.602G>A	XP_016874282.1:p.Ser201Asn
XR_002957287.1:n.625G>A
XR_944496.2:n.775G>A
NM_145648.4:c.602G>A MANE Select	NP_663623.1:p.Ser201Asn