Canonical Allele Identifier: CA1541437430
Gene: C7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.40964658A= , CM000667.2:g.40964658A= GRCh38
NC_000005.9:g.40964760A= , CM000667.1:g.40964760A= GRCh37
NC_000005.8:g.41000517A= NCBI36
NG_011692.1:g.60162A= , LRG_30:g.60162A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000486779.2:n.459A=
ENST00000696333.1:c.1750-83A= ENSP00000512566.1:n.1750-83A=
ENST00000696441.1:c.1750-83A= ENSP00000512631.1:n.1750-83A=
ENST00000706664.1:n.1864-83A=
ENST00000706666.1:n.1826-83A=
ENST00000706667.1:n.2640-83A=
ENST00000706668.1:n.2478-83A=
ENST00000313164.10:c.1750-83A= MANE Select ENSP00000322061.9:n.1750-83A=
ENST00000313164.9:c.1750-83A= ENSP00000322061.9:n.1750-83A=
ENST00000486779.1:n.180A=
NM_000587.2:c.1750-83A= , LRG_30t1:c.1750-83A= NP_000578.2:n.1750-83A=
XM_011514122.1:c.1750-83A= XP_011512424.1:n.1750-83A=
NM_000587.3:c.1750-83A= NP_000578.2:n.1750-83A=
NM_000587.4:c.1750-83A= MANE Select NP_000578.2:n.1750-83A=