Canonical Allele Identifier: CA3164986860

Gene: LRRC14 LRRC24

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144524374T= , CM000670.2:g.144524374T=	GRCh38
NC_000008.10:g.145749758T= , CM000670.1:g.145749758T=	GRCh37
NC_000008.9:g.145720566T=	NCBI36
NG_033083.1:g.11410T=

Transcript Alleles

HGVS	Amino-acid Change
NM_001024678.4:c.438+67A= (LRRC24) MANE Select	NP_001019849.2:n.438+67A=
NM_014665.4:c.*2896T= (LRRC14) MANE Select	NP_055480.1:n.*2896T=
ENST00000292524.6:c.*2896T= (LRRC14) MANE Select	ENSP00000292524.1:n.*2896T=
ENST00000529415.7:c.438+67A= (LRRC24) MANE Select	ENSP00000434849.1:n.438+67A=
NM_001024678.3:c.438+67A= (LRRC24)	NP_001019849.2:n.438+67A=
NM_001272036.1:c.*2896T= (LRRC14)	NP_001258965.1:n.*2896T=
NM_001272036.2:c.*2896T= (LRRC14)	NP_001258965.1:n.*2896T=
NM_014665.3:c.*2896T= (LRRC14)	NP_055480.1:n.*2896T=
ENST00000292524.5:c.*2896T= (LRRC14)	ENSP00000292524.1:n.*2896T=
ENST00000528528.1:n.1336T= (LRRC14)
ENST00000529415.6:c.438+67A= (LRRC24)	ENSP00000434849.1:n.438+67A=
ENST00000529995.1:n.443T= (LRRC14)
ENST00000533758.1:c.438+67A= (LRRC24)	ENSP00000435653.1:n.438+67A=
XM_005272358.3:c.*2896T= (LRRC14)	XP_005272415.1:n.*2896T=
XM_005272359.3:c.*2896T= (LRRC14)	XP_005272416.1:n.*2896T=
XM_005272360.3:c.*2896T= (LRRC14)	XP_005272417.1:n.*2896T=
XM_005272361.2:c.*2896T= (LRRC14)	XP_005272418.1:n.*2896T=
XM_011517387.1:c.*2896T= (LRRC14)	XP_011515689.1:n.*2896T=
XM_011517388.1:c.*2896T= (LRRC14)	XP_011515690.1:n.*2896T=
XR_928369.1:n.4222T= (LRRC14)
XR_928370.1:n.4369T= (LRRC14)
XR_928371.1:n.4410T= (LRRC14)