Canonical Allele Identifier: CA127332

Gene: RHCE

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.25390874C= , CM000663.2:g.25390874C=	GRCh38
NC_000001.10:g.25717365C= , CM000663.1:g.25717365C=	GRCh37
NC_000001.9:g.25589952C=	NCBI36
NG_009208.3:g.44319G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294413.13:c.676G= MANE Select	ENSP00000294413.6:p.Ala226=
ENST00000243186.10:c.676G=	ENSP00000243186.7:p.Ala226=
ENST00000294413.11:c.676G=	ENSP00000294413.6:p.Ala226=
ENST00000340849.8:c.487-1761G=	ENSP00000345084.4:n.487-1761G=
ENST00000346452.8:c.487-5030G=	ENSP00000344485.4:n.487-5030G=
ENST00000349320.7:c.628G=	ENSP00000311185.4:p.Ala210=
ENST00000349438.8:c.676G=	ENSP00000334570.5:p.Ala226=
ENST00000374352.6:c.676G=	ENSP00000363472.3:p.Ala226=
ENST00000413854.5:c.676G=	ENSP00000415417.2:p.Ala226=
ENST00000527187.5:n.831G=
ENST00000527747.5:c.107+11722G=
ENST00000533771.1:c.*132-1761G=	ENSP00000435401.1:n.*132-1761G=
NM_020485.4:c.676G=	NP_065231.3:p.Ala226=
NM_138616.3:c.487-5030G=	NP_619522.3:n.487-5030G=
NM_138617.3:c.487-1761G=	NP_619523.3:n.487-1761G=
NM_138618.3:c.676G=	NP_619524.3:p.Ala226=
XM_005245957.2:c.676G=	XP_005246014.1:p.Ala226=
XM_006710810.2:c.676G=	XP_006710873.1:p.Ala226=
XM_011541888.1:c.556G=	XP_011540190.1:p.Ala186=
XM_011541889.1:c.547G=	XP_011540191.1:p.Ala183=
XM_011541890.1:c.676G=	XP_011540192.1:p.Ala226=
XM_011541891.1:c.508G=	XP_011540193.1:p.Ala170=
NM_001330430.2:c.676G=	NP_001317359.1:p.Ala226=
NM_020485.5:c.676G=	NP_065231.3:p.Ala226=
NM_138616.4:c.487-5030G=	NP_619522.3:n.487-5030G=
NM_138617.4:c.487-1761G=	NP_619523.3:n.487-1761G=
NM_138618.5:c.676G=	NP_619524.5:p.Ala226=
XM_005245957.4:c.676G=	XP_005246014.1:p.Ala226=
XM_006710810.3:c.676G=	XP_006710873.1:p.Ala226=
XM_011541888.3:c.556G=	XP_011540190.1:p.Ala186=
XM_011541889.3:c.781G=	XP_011540191.2:p.Ala261=
XM_011541891.3:c.508G=	XP_011540193.1:p.Ala170=
XM_017002014.2:c.676G=	XP_016857503.1:p.Ala226=
NM_001330430.4:c.676G=	NP_001317359.1:p.Ala226=
NM_020485.7:c.-4294966581G=
NM_138616.5:c.487-5030G=	NP_619522.3:n.487-5030G=
NM_138617.5:c.487-1761G=	NP_619523.3:n.487-1761G=
NM_138618.6:c.676G=	NP_619524.5:p.Ala226=
NM_020485.8:c.676G= MANE Select	NP_065231.4:p.Ala226=