Canonical Allele Identifier: CA1541437423

Gene: C7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.40964651A= , CM000667.2:g.40964651A=	GRCh38
NC_000005.9:g.40964753A= , CM000667.1:g.40964753A=	GRCh37
NC_000005.8:g.41000510A=	NCBI36
NG_011692.1:g.60155A= , LRG_30:g.60155A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000486779.2:n.452A=
ENST00000696333.1:c.1750-90A=	ENSP00000512566.1:n.1750-90A=
ENST00000696441.1:c.1750-90A=	ENSP00000512631.1:n.1750-90A=
ENST00000706664.1:n.1864-90A=
ENST00000706666.1:n.1826-90A=
ENST00000706667.1:n.2640-90A=
ENST00000706668.1:n.2478-90A=
ENST00000313164.10:c.1750-90A= MANE Select	ENSP00000322061.9:n.1750-90A=
ENST00000313164.9:c.1750-90A=	ENSP00000322061.9:n.1750-90A=
ENST00000486779.1:n.173A=
NM_000587.2:c.1750-90A= , LRG_30t1:c.1750-90A=	NP_000578.2:n.1750-90A=
XM_011514122.1:c.1750-90A=	XP_011512424.1:n.1750-90A=
NM_000587.3:c.1750-90A=	NP_000578.2:n.1750-90A=
NM_000587.4:c.1750-90A= MANE Select	NP_000578.2:n.1750-90A=