Canonical Allele Identifier: CA3043118
Community Standard Title: NM_198506.5(LRIT3):c.1029G>T (p.Val343=)
Gene: LRIT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.109869778G>T , CM000666.2:g.109869778G>T GRCh38
NC_000004.11:g.110790934G>T , CM000666.1:g.110790934G>T GRCh37
NC_000004.10:g.111010383G>T NCBI36
NG_033249.1:g.26595G>T

Transcript Alleles

HGVS Amino-acid Change
NM_198506.5:c.1029G>T MANE Select NP_940908.3:p.Val343=
ENST00000594814.6:c.1029G>T MANE Select ENSP00000469759.1:p.Val343=
NM_198506.4:c.1029G>T NP_940908.3:p.Val343=
ENST00000327908.3:c.480G>T ENSP00000328222.3:p.Val160=
ENST00000594814.5:c.1029G>T ENSP00000469759.1:p.Val343=
XM_005262979.2:c.480G>T XP_005263036.1:p.Val160=
XM_017008167.1:c.480G>T XP_016863656.1:p.Val160=