Canonical Allele Identifier: CA103732121
Community Standard Title: NM_198506.5(LRIT3):c.492A>G (p.Arg164=)
Gene: LRIT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.109851879A>G , CM000666.2:g.109851879A>G GRCh38
NC_000004.11:g.110773035A>G , CM000666.1:g.110773035A>G GRCh37
NC_000004.10:g.110992484A>G NCBI36
NG_033249.1:g.8696A>G

Transcript Alleles

HGVS Amino-acid Change
NM_198506.5:c.492A>G MANE Select NP_940908.3:p.Arg164=
ENST00000594814.6:c.492A>G MANE Select ENSP00000469759.1:p.Arg164=
NM_198506.4:c.492A>G NP_940908.3:p.Arg164=
ENST00000327908.3:c.-215A>G ENSP00000328222.3:n.-215A>G
ENST00000594814.5:c.492A>G ENSP00000469759.1:p.Arg164=
XM_005262979.2:c.-215A>G XP_005263036.1:n.-215A>G
XM_017008168.1:c.492A>G XP_016863657.1:p.Arg164=