Canonical Allele Identifier: CA3043240
Community Standard Title: NM_198506.5(LRIT3):c.1677G>A (p.Val559=)
Gene: LRIT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.109870426G>A , CM000666.2:g.109870426G>A GRCh38
NC_000004.11:g.110791582G>A , CM000666.1:g.110791582G>A GRCh37
NC_000004.10:g.111011031G>A NCBI36
NG_033249.1:g.27243G>A

Transcript Alleles

HGVS Amino-acid Change
NM_198506.5:c.1677G>A MANE Select NP_940908.3:p.Val559=
ENST00000594814.6:c.1677G>A MANE Select ENSP00000469759.1:p.Val559=
NM_198506.4:c.1677G>A NP_940908.3:p.Val559=
ENST00000327908.3:c.1128G>A ENSP00000328222.3:p.Val376=
ENST00000594814.5:c.1677G>A ENSP00000469759.1:p.Val559=
XM_005262979.2:c.1128G>A XP_005263036.1:p.Val376=
XM_017008167.1:c.1128G>A XP_016863656.1:p.Val376=