Canonical Allele Identifier: CA381495513

Gene: LRFN4 PC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66860169G>T , CM000673.2:g.66860169G>T	GRCh38
NC_000011.9:g.66627640G>T , CM000673.1:g.66627640G>T	GRCh37
NC_000011.8:g.66384216G>T	NCBI36
NG_008319.1:g.103208C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001040716.2:c.1368+3605C>A (PC) MANE Select	NP_001035806.1:n.1368+3605C>A
NM_024036.5:c.1882G>T (LRFN4) MANE Select	NP_076941.2:p.Glu628Ter
ENST00000309602.5:c.1882G>T (LRFN4) MANE Select	ENSP00000312535.4:p.Glu628Ter
ENST00000393960.7:c.1368+3605C>A (PC) MANE Select	ENSP00000377532.1:n.1368+3605C>A
NM_000920.3:c.1368+3605C>A (PC)	NP_000911.2:n.1368+3605C>A
NM_000920.4:c.1368+3605C>A (PC)	NP_000911.2:n.1368+3605C>A
NM_001040716.1:c.1368+3605C>A (PC)	NP_001035806.1:n.1368+3605C>A
NM_001363524.1:c.1882G>T (LRFN4)	NP_001350453.1:p.Glu628Ter
NM_001363524.2:c.1882G>T (LRFN4)	NP_001350453.1:p.Glu628Ter
NM_022172.2:c.1368+3605C>A (PC)	NP_071504.2:n.1368+3605C>A
NM_022172.3:c.1368+3605C>A (PC)	NP_071504.2:n.1368+3605C>A
NM_024036.4:c.1882G>T (LRFN4)	NP_076941.2:p.Glu628Ter
ENST00000309602.4:c.1882G>T (LRFN4)	ENSP00000312535.4:p.Glu628Ter
ENST00000393952.3:c.1133-78G>T (LRFN4)	ENSP00000377524.3:n.1133-78G>T
ENST00000393955.6:c.1368+3605C>A (PC)	ENSP00000377527.2:n.1368+3605C>A
ENST00000393958.6:c.1368+3605C>A (PC)	ENSP00000377530.2:n.1368+3605C>A
ENST00000393958.7:c.1368+3605C>A (PC)	ENSP00000377530.2:n.1368+3605C>A
ENST00000393960.5:c.1368+3605C>A (PC)	ENSP00000377532.1:n.1368+3605C>A
ENST00000525476.2:n.290-10104C>A (PC)
ENST00000528224.2:c.1368+3605C>A (PC)	ENSP00000498317.1:n.1368+3605C>A
ENST00000528403.6:c.1368+3605C>A (PC)	ENSP00000498816.1:n.1368+3605C>A
ENST00000529047.6:c.1368+3605C>A (PC)	ENSP00000435905.2:n.1368+3605C>A
ENST00000530187.1:n.213+94C>A (PC)
ENST00000651036.1:c.1368+3605C>A (PC)	ENSP00000498406.1:n.1368+3605C>A
ENST00000651469.1:c.1368+3605C>A (PC)	ENSP00000498712.1:n.1368+3605C>A
ENST00000651854.1:c.1368+3605C>A (PC)	ENSP00000498994.1:n.1368+3605C>A
ENST00000652125.1:c.1368+3605C>A (PC)	ENSP00000498302.1:n.1368+3605C>A
XM_005274031.3:c.1368+3605C>A (PC)	XP_005274088.1:n.1368+3605C>A
XM_005274031.4:c.1368+3605C>A (PC)	XP_005274088.1:n.1368+3605C>A
XM_005274032.3:c.1368+3605C>A (PC)	XP_005274089.1:n.1368+3605C>A
XM_005274032.4:c.1368+3605C>A (PC)	XP_005274089.1:n.1368+3605C>A
XM_005274239.2:c.1882G>T (LRFN4)	XP_005274296.1:p.Glu628Ter
XM_006718577.2:c.1368+3605C>A (PC)	XP_006718640.1:n.1368+3605C>A
XM_006718578.2:c.1368+3605C>A (PC)	XP_006718641.1:n.1368+3605C>A
XM_006718578.3:c.1368+3605C>A (PC)	XP_006718641.1:n.1368+3605C>A
XM_011545085.1:c.1368+3605C>A (PC)	XP_011543387.1:n.1368+3605C>A
XM_011545086.1:c.1368+3605C>A (PC)	XP_011543388.1:n.1368+3605C>A
XM_011545086.2:c.1368+3605C>A (PC)	XP_011543388.1:n.1368+3605C>A
XM_017017868.1:c.1368+3605C>A (PC)	XP_016873357.1:n.1368+3605C>A
XM_017017869.1:c.1368+3605C>A (PC)	XP_016873358.1:n.1368+3605C>A
XM_017017870.1:c.1368+3605C>A (PC)	XP_016873359.1:n.1368+3605C>A
XM_017017871.1:c.1368+3605C>A (PC)	XP_016873360.1:n.1368+3605C>A
XM_017017872.2:c.1368+3605C>A (PC)	XP_016873361.1:n.1368+3605C>A