Canonical Allele Identifier: CA1541437442

Gene: C7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.40964671_40964672delinsAT , CM000667.2:g.40964671_40964672delinsAT	GRCh38
NC_000005.9:g.40964773_40964774delinsAT , CM000667.1:g.40964773_40964774delinsAT	GRCh37
NC_000005.8:g.41000530_41000531delinsAT	NCBI36
NG_011692.1:g.60175_60176delinsAT , LRG_30:g.60175_60176delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000486779.2:n.472_473delinsAT
ENST00000696333.1:c.1750-70_1750-69delinsAT	ENSP00000512566.1:n.1750-70_1750-69delinsAT
ENST00000696441.1:c.1750-70_1750-69delinsAT	ENSP00000512631.1:n.1750-70_1750-69delinsAT
ENST00000706664.1:n.1864-70_1864-69delinsAT
ENST00000706666.1:n.1826-70_1826-69delinsAT
ENST00000706667.1:n.2640-70_2640-69delinsAT
ENST00000706668.1:n.2478-70_2478-69delinsAT
ENST00000313164.10:c.1750-70_1750-69delinsAT MANE Select	ENSP00000322061.9:n.1750-70_1750-69delinsAT
ENST00000313164.9:c.1750-70_1750-69delinsAT	ENSP00000322061.9:n.1750-70_1750-69delinsAT
ENST00000486779.1:n.193_194delinsAT
NM_000587.2:c.1750-70_1750-69delinsAT , LRG_30t1:c.1750-70_1750-69delinsAT	NP_000578.2:n.1750-70_1750-69delinsAT
XM_011514122.1:c.1750-70_1750-69delinsAT	XP_011512424.1:n.1750-70_1750-69delinsAT
NM_000587.3:c.1750-70_1750-69delinsAT	NP_000578.2:n.1750-70_1750-69delinsAT
NM_000587.4:c.1750-70_1750-69delinsAT MANE Select	NP_000578.2:n.1750-70_1750-69delinsAT