Canonical Allele Identifier: CA1541437450

Gene: C7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.40964672T= , CM000667.2:g.40964672T=	GRCh38
NC_000005.9:g.40964774T= , CM000667.1:g.40964774T=	GRCh37
NC_000005.8:g.41000531T=	NCBI36
NG_011692.1:g.60176T= , LRG_30:g.60176T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000486779.2:n.473T=
ENST00000696333.1:c.1750-69T=	ENSP00000512566.1:n.1750-69T=
ENST00000696441.1:c.1750-69T=	ENSP00000512631.1:n.1750-69T=
ENST00000706664.1:n.1864-69T=
ENST00000706666.1:n.1826-69T=
ENST00000706667.1:n.2640-69T=
ENST00000706668.1:n.2478-69T=
ENST00000313164.10:c.1750-69T= MANE Select	ENSP00000322061.9:n.1750-69T=
ENST00000313164.9:c.1750-69T=	ENSP00000322061.9:n.1750-69T=
ENST00000486779.1:n.194T=
NM_000587.2:c.1750-69T= , LRG_30t1:c.1750-69T=	NP_000578.2:n.1750-69T=
XM_011514122.1:c.1750-69T=	XP_011512424.1:n.1750-69T=
NM_000587.3:c.1750-69T=	NP_000578.2:n.1750-69T=
NM_000587.4:c.1750-69T= MANE Select	NP_000578.2:n.1750-69T=