Canonical Allele Identifier: CA1419595626

Gene: LRRC34

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169796851_169796853delinsGAC , CM000665.2:g.169796851_169796853delinsGAC	GRCh38
NC_000003.11:g.169514639_169514641delinsGAC , CM000665.1:g.169514639_169514641delinsGAC	GRCh37
NC_000003.10:g.170997333_170997335delinsGAC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000446859.7:c.800_802delinsGTC MANE Select	ENSP00000414635.1:p.Cys267=
ENST00000446859.5:c.800_802delinsGTC	ENSP00000414635.1:p.Cys267=
ENST00000522080.5:n.777_779delinsGTC
ENST00000522329.1:n.49_51delinsGTC
ENST00000522526.6:c.704_706delinsGTC	ENSP00000429278.2:p.Cys235=
ENST00000522596.6:n.782_784delinsGTC
ENST00000522830.5:c.617_619delinsGTC	ENSP00000429593.1:p.Cys206=
ENST00000524054.5:n.648_650delinsGTC
ENST00000524327.5:n.600_602delinsGTC
ENST00000528597.1:c.47_49delinsGTC	ENSP00000436883.1:p.Cys16=
ENST00000602774.1:n.186_188delinsGTC
NM_001172779.1:c.800_802delinsGTC	NP_001166250.1:p.Cys267=
NM_001172780.1:c.800_802delinsGTC	NP_001166251.1:p.Cys267=
NM_153353.4:c.704_706delinsGTC	NP_699184.2:p.Cys235=
XM_005247133.2:c.617_619delinsGTC	XP_005247190.1:p.Cys206=
XM_006713508.2:c.746_748delinsGTC	XP_006713571.1:p.Cys249=
XM_011512442.1:c.797_799delinsGTC	XP_011510744.1:p.Cys266=
NM_001363888.1:c.617_619delinsGTC	NP_001350817.1:p.Cys206=
XM_006713508.4:c.746_748delinsGTC	XP_006713571.1:p.Cys249=
XM_011512442.2:c.797_799delinsGTC	XP_011510744.1:p.Cys266=
XM_017005746.1:c.614_616delinsGTC	XP_016861235.1:p.Cys205=
NM_001172779.2:c.800_802delinsGTC MANE Select	NP_001166250.1:p.Cys267=
NM_001172780.2:c.800_802delinsGTC	NP_001166251.1:p.Cys267=
NM_001363888.2:c.617_619delinsGTC	NP_001350817.1:p.Cys206=
NM_001370608.1:c.614_616delinsGTC	NP_001357537.1:p.Cys205=
NM_001370609.1:c.617_619delinsGTC	NP_001357538.1:p.Cys206=
NM_153353.5:c.704_706delinsGTC	NP_699184.2:p.Cys235=