Canonical Allele Identifier: CA2071402037

Gene: SLC15A4

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128814894_128814908delinsGAGGAAGACCACAAA , CM000674.2:g.128814894_128814908delinsGAGGAAGACCACAAA	GRCh38
NC_000012.11:g.129299439_129299453delinsGAGGAAGACCACAAA , CM000674.1:g.129299439_129299453delinsGAGGAAGACCACAAA	GRCh37
NC_000012.10:g.127865392_127865406delinsGAGGAAGACCACAAA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266771.10:c.709_723delinsTTTGTGGTCTTCCTC MANE Select	ENSP00000266771.5:p.Phe237=
ENST00000266771.9:c.709_723delinsTTTGTGGTCTTCCTC	ENSP00000266771.5:p.Phe237=
ENST00000366292.6:n.1021_1035delinsTTTGTGGTCTTCCTC
ENST00000376740.8:c.288_302delinsTTTGTGGTCTTCCTC
ENST00000376744.8:c.545_559delinsTTTGTGGTCTTCCTC
ENST00000539703.1:n.359_373delinsTTTGTGGTCTTCCTC
ENST00000614634.1:c.-134_-120delinsTTTGTGGTCTTCCTC	ENSP00000483143.1:n.-134_-120delinsTTTGTGGTCTTCCTC
NM_145648.3:c.709_723delinsTTTGTGGTCTTCCTC	NP_663623.1:p.Phe237=
XM_011537895.1:c.859_873delinsTTTGTGGTCTTCCTC	XP_011536197.1:p.Phe287=
XR_429081.2:n.732_746delinsTTTGTGGTCTTCCTC
XR_944494.1:n.882_896delinsTTTGTGGTCTTCCTC
XR_944495.1:n.882_896delinsTTTGTGGTCTTCCTC
XR_944496.1:n.882_896delinsTTTGTGGTCTTCCTC
XR_944497.1:n.882_896delinsTTTGTGGTCTTCCTC
XM_017018791.1:c.859_873delinsTTTGTGGTCTTCCTC	XP_016874280.1:p.Phe287=
XM_017018792.1:c.859_873delinsTTTGTGGTCTTCCTC	XP_016874281.1:p.Phe287=
XM_017018793.1:c.709_723delinsTTTGTGGTCTTCCTC	XP_016874282.1:p.Phe237=
XR_002957287.1:n.732_746delinsTTTGTGGTCTTCCTC
XR_944496.2:n.882_896delinsTTTGTGGTCTTCCTC
NM_145648.4:c.709_723delinsTTTGTGGTCTTCCTC MANE Select	NP_663623.1:p.Phe237=