Canonical Allele Identifier: CA357873232

Gene: LRIT3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.109870715C>G , CM000666.2:g.109870715C>G	GRCh38
NC_000004.11:g.110791871C>G , CM000666.1:g.110791871C>G	GRCh37
NC_000004.10:g.111011320C>G	NCBI36
NG_033249.1:g.27532C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_198506.5:c.1966C>G MANE Select	NP_940908.3:p.Leu656Val
ENST00000594814.6:c.1966C>G MANE Select	ENSP00000469759.1:p.Leu656Val
NM_198506.4:c.1966C>G	NP_940908.3:p.Leu656Val
ENST00000327908.3:c.1417C>G	ENSP00000328222.3:p.Leu473Val
ENST00000594814.5:c.1966C>G	ENSP00000469759.1:p.Leu656Val
XM_005262979.2:c.1417C>G	XP_005263036.1:p.Leu473Val
XM_017008167.1:c.1417C>G	XP_016863656.1:p.Leu473Val