Canonical Allele Identifier: CA1610190131

Gene: GCM2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10874357T= , CM000668.2:g.10874357T=	GRCh38
NC_000006.11:g.10874590T= , CM000668.1:g.10874590T=	GRCh37
NC_000006.10:g.10982576T=	NCBI36
NG_008970.1:g.12509A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000379491.5:c.1159A= MANE Select	ENSP00000368805.4:p.Thr387=
ENST00000379491.4:c.1159A=	ENSP00000368805.4:p.Thr387=
ENST00000480294.1:c.101-17156T=	ENSP00000417929.1:n.101-17156T=
NM_004752.3:c.1159A=	NP_004743.1:p.Thr387=
XM_011514991.1:c.1159A=	XP_011513293.1:p.Thr387=
NM_004752.4:c.1159A= MANE Select	NP_004743.1:p.Thr387=