Canonical Allele Identifier: CA1362098470

Gene: CCRL2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46408373G= , CM000665.2:g.46408373G=	GRCh38
NC_000003.11:g.46449864G= , CM000665.1:g.46449864G=	GRCh37
NC_000003.10:g.46424868G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_003965.5:c.294G= MANE Select	NP_003956.2:p.Gly98=
ENST00000399036.4:c.294G= MANE Select	ENSP00000381994.3:p.Gly98=
NM_001130910.1:c.330G=	NP_001124382.1:p.Gly110=
NM_001130910.2:c.330G=	NP_001124382.1:p.Gly110=
NM_003965.4:c.294G=	NP_003956.2:p.Gly98=
ENST00000357392.4:c.330G=	ENSP00000349967.4:p.Gly110=
ENST00000399036.3:c.294G=	ENSP00000381994.3:p.Gly98=
ENST00000400880.3:c.294G=	ENSP00000383677.3:p.Gly98=
ENST00000400882.2:c.294G=	ENSP00000383678.2:p.Gly98=
ENST00000433848.1:c.294G=	ENSP00000414957.1:p.Gly98=
XM_011534208.1:c.294G=	XP_011532510.1:p.Gly98=
XM_011534209.1:c.294G=	XP_011532511.1:p.Gly98=
XM_017007436.1:c.294G=	XP_016862925.1:p.Gly98=