Canonical Allele Identifier: CA1541437982

Gene: C7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.40964970G= , CM000667.2:g.40964970G=	GRCh38
NC_000005.9:g.40965072G= , CM000667.1:g.40965072G=	GRCh37
NC_000005.8:g.41000829G=	NCBI36
NG_011692.1:g.60474G= , LRG_30:g.60474G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000486779.2:n.674+97G=
ENST00000696333.1:c.1882+97G=	ENSP00000512566.1:n.1882+97G=
ENST00000696441.1:c.1882+97G=	ENSP00000512631.1:n.1882+97G=
ENST00000706664.1:n.1996+97G=
ENST00000706666.1:n.1958+97G=
ENST00000706667.1:n.2772+97G=
ENST00000706668.1:n.2610+97G=
ENST00000313164.10:c.1882+97G= MANE Select	ENSP00000322061.9:n.1882+97G=
ENST00000313164.9:c.1882+97G=	ENSP00000322061.9:n.1882+97G=
ENST00000486779.1:n.395+97G=
NM_000587.2:c.1882+97G= , LRG_30t1:c.1882+97G=	NP_000578.2:n.1882+97G=
XM_011514122.1:c.1882+97G=	XP_011512424.1:n.1882+97G=
NM_000587.3:c.1882+97G=	NP_000578.2:n.1882+97G=
NM_000587.4:c.1882+97G= MANE Select	NP_000578.2:n.1882+97G=