Canonical Allele Identifier: CA2071402526
Gene: SLC15A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.128815158_128815160delinsGTT , CM000674.2:g.128815158_128815160delinsGTT GRCh38
NC_000012.11:g.129299703_129299705delinsGTT , CM000674.1:g.129299703_129299705delinsGTT GRCh37
NC_000012.10:g.127865656_127865658delinsGTT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266771.10:c.547-90_547-88delinsAAC MANE Select ENSP00000266771.5:n.547-90_547-88delinsAAC
ENST00000266771.9:c.547-90_547-88delinsAAC ENSP00000266771.5:n.547-90_547-88delinsAAC
ENST00000366292.6:n.769_771delinsAAC
ENST00000376740.8:c.126-90_126-88delinsAAC
ENST00000376744.8:c.383-90_383-88delinsAAC
ENST00000535272.1:n.341-90_341-88delinsAAC
ENST00000539703.1:n.197-90_197-88delinsAAC
NM_145648.3:c.547-90_547-88delinsAAC NP_663623.1:n.547-90_547-88delinsAAC
XM_011537895.1:c.697-90_697-88delinsAAC XP_011536197.1:n.697-90_697-88delinsAAC
XR_429081.2:n.570-90_570-88delinsAAC
XR_944494.1:n.720-90_720-88delinsAAC
XR_944495.1:n.720-90_720-88delinsAAC
XR_944496.1:n.720-90_720-88delinsAAC
XR_944497.1:n.720-90_720-88delinsAAC
XM_017018791.1:c.697-90_697-88delinsAAC XP_016874280.1:n.697-90_697-88delinsAAC
XM_017018792.1:c.697-90_697-88delinsAAC XP_016874281.1:n.697-90_697-88delinsAAC
XM_017018793.1:c.547-90_547-88delinsAAC XP_016874282.1:n.547-90_547-88delinsAAC
XR_002957287.1:n.570-90_570-88delinsAAC
XR_944496.2:n.720-90_720-88delinsAAC
NM_145648.4:c.547-90_547-88delinsAAC MANE Select NP_663623.1:n.547-90_547-88delinsAAC