Canonical Allele Identifier: CA1541437958

Gene: C7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.40964954T= , CM000667.2:g.40964954T=	GRCh38
NC_000005.9:g.40965056T= , CM000667.1:g.40965056T=	GRCh37
NC_000005.8:g.41000813T=	NCBI36
NG_011692.1:g.60458T= , LRG_30:g.60458T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000486779.2:n.674+81T=
ENST00000696333.1:c.1882+81T=	ENSP00000512566.1:n.1882+81T=
ENST00000696441.1:c.1882+81T=	ENSP00000512631.1:n.1882+81T=
ENST00000706664.1:n.1996+81T=
ENST00000706666.1:n.1958+81T=
ENST00000706667.1:n.2772+81T=
ENST00000706668.1:n.2610+81T=
ENST00000313164.10:c.1882+81T= MANE Select	ENSP00000322061.9:n.1882+81T=
ENST00000313164.9:c.1882+81T=	ENSP00000322061.9:n.1882+81T=
ENST00000486779.1:n.395+81T=
NM_000587.2:c.1882+81T= , LRG_30t1:c.1882+81T=	NP_000578.2:n.1882+81T=
XM_011514122.1:c.1882+81T=	XP_011512424.1:n.1882+81T=
NM_000587.3:c.1882+81T=	NP_000578.2:n.1882+81T=
NM_000587.4:c.1882+81T= MANE Select	NP_000578.2:n.1882+81T=