Canonical Allele Identifier: CA1541545702

Gene: C6

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.41213252A= , CM000667.2:g.41213252A=	GRCh38
NC_000005.9:g.41213354A= , CM000667.1:g.41213354A=	GRCh37
NC_000005.8:g.41249111A=	NCBI36
NG_011582.1:g.53187T= , LRG_29:g.53187T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433294.2:c.-178+124T=	ENSP00000401578.2:n.-178+124T=
ENST00000706655.1:n.253+124T=
ENST00000706656.1:n.157+124T=
ENST00000337836.10:c.-21+124T= MANE Select	ENSP00000338861.5:n.-21+124T=
ENST00000263413.7:c.-20-10002T=	ENSP00000263413.3:n.-20-10002T=
ENST00000337836.9:c.-21+124T=	ENSP00000338861.5:n.-21+124T=
ENST00000433294.1:c.-178+124T=	ENSP00000401578.1:n.-178+124T=
NM_000065.3:c.-21+124T=	NP_000056.2:n.-21+124T=
NM_001115131.2:c.-20-10002T=	NP_001108603.2:n.-20-10002T=
XM_005248357.1:c.8-10002T=	XP_005248414.1:n.8-10002T=
XM_006714496.2:c.8-10002T=	XP_006714559.1:n.8-10002T=
XM_011514114.1:c.8-10002T=	XP_011512416.1:n.8-10002T=
XM_011514115.1:c.-21+124T=	XP_011512417.1:n.-21+124T=
XM_011514116.1:c.-159+124T=	XP_011512418.1:n.-159+124T=
XM_011514117.1:c.-178+124T=	XP_011512419.1:n.-178+124T=
XM_011514119.1:c.8-10002T=	XP_011512421.1:n.8-10002T=
XM_011514120.1:c.8-10002T=	XP_011512422.1:n.8-10002T=
XM_005248357.3:c.8-10002T=	XP_005248414.1:n.8-10002T=
XM_006714496.4:c.8-10002T=	XP_006714559.1:n.8-10002T=
XM_011514114.3:c.8-10002T=	XP_011512416.1:n.8-10002T=
XM_011514115.3:c.-21+124T=	XP_011512417.1:n.-21+124T=
XM_011514116.3:c.-159+124T=	XP_011512418.1:n.-159+124T=
XM_011514117.3:c.-178+124T=	XP_011512419.1:n.-178+124T=
XM_011514119.3:c.8-10002T=	XP_011512421.1:n.8-10002T=
XM_017009818.2:c.-182+124T=	XP_016865307.1:n.-182+124T=
NM_000065.4:c.-21+124T=	NP_000056.2:n.-21+124T=
NM_001115131.3:c.-20-10002T=	NP_001108603.2:n.-20-10002T=
NM_000065.5:c.-21+124T= MANE Select	NP_000056.2:n.-21+124T=
NM_001115131.4:c.-20-10002T=	NP_001108603.2:n.-20-10002T=