Canonical Allele Identifier: CA2406838880

Gene: CYB5R3

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42630594_42630595delinsAG , CM000684.2:g.42630594_42630595delinsAG	GRCh38
NC_000022.10:g.43026600_43026601delinsAG , CM000684.1:g.43026600_43026601delinsAG	GRCh37
NC_000022.9:g.41356544_41356545delinsAG	NCBI36
NG_012194.1:g.23805_23806delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361740.9:c.333+287_333+288delinsCT	ENSP00000354468.5:n.333+287_333+288delinsCT
ENST00000402438.6:c.264+287_264+288delinsCT	ENSP00000385679.1:n.264+287_264+288delinsCT
ENST00000407332.6:c.351+287_351+288delinsCT	ENSP00000384457.2:n.351+287_351+288delinsCT
ENST00000407623.8:c.264+287_264+288delinsCT	ENSP00000384834.3:n.264+287_264+288delinsCT
ENST00000438270.2:c.264+287_264+288delinsCT	ENSP00000403439.2:n.264+287_264+288delinsCT
ENST00000686129.1:c.264+287_264+288delinsCT	ENSP00000508623.1:n.264+287_264+288delinsCT
ENST00000686523.1:c.*282+287_*282+288delinsCT	ENSP00000508940.1:n.*282+287_*282+288delinsCT
ENST00000687183.1:n.394+287_394+288delinsCT
ENST00000687198.1:c.264+287_264+288delinsCT	ENSP00000508492.1:n.264+287_264+288delinsCT
ENST00000688117.1:c.432+287_432+288delinsCT	ENSP00000509015.1:n.432+287_432+288delinsCT
ENST00000688244.1:c.333+287_333+288delinsCT	ENSP00000510355.1:n.333+287_333+288delinsCT
ENST00000689001.1:n.740+287_740+288delinsCT
ENST00000689195.1:c.333+287_333+288delinsCT	ENSP00000509895.1:n.333+287_333+288delinsCT
ENST00000689239.1:n.500+287_500+288delinsCT
ENST00000689795.1:n.495+287_495+288delinsCT
ENST00000690835.1:c.333+287_333+288delinsCT	ENSP00000509038.1:n.333+287_333+288delinsCT
ENST00000690993.1:n.410+287_410+288delinsCT
ENST00000691295.1:c.333+287_333+288delinsCT	ENSP00000508706.1:n.333+287_333+288delinsCT
ENST00000691918.1:c.312+287_312+288delinsCT	ENSP00000509525.1:n.312+287_312+288delinsCT
ENST00000692152.1:c.264+287_264+288delinsCT	ENSP00000509317.1:n.264+287_264+288delinsCT
ENST00000692344.1:n.357+287_357+288delinsCT
ENST00000693157.1:c.253+287_253+288delinsCT	ENSP00000510610.1:n.253+287_253+288delinsCT
ENST00000693363.1:c.333+287_333+288delinsCT	ENSP00000510411.1:n.333+287_333+288delinsCT
ENST00000693367.1:c.333+287_333+288delinsCT	ENSP00000508815.1:n.333+287_333+288delinsCT
ENST00000693639.1:c.326+287_326+288delinsCT	ENSP00000510223.1:n.326+287_326+288delinsCT
ENST00000693646.1:c.239+287_239+288delinsCT	ENSP00000508449.1:n.239+287_239+288delinsCT
ENST00000352397.10:c.333+287_333+288delinsCT MANE Select	ENSP00000338461.6:n.333+287_333+288delinsCT
ENST00000352397.9:c.333+287_333+288delinsCT	ENSP00000338461.6:n.333+287_333+288delinsCT
ENST00000361740.8:c.432+287_432+288delinsCT	ENSP00000354468.4:n.432+287_432+288delinsCT
ENST00000402438.5:c.264+287_264+288delinsCT	ENSP00000385679.1:n.264+287_264+288delinsCT
ENST00000407332.5:c.264+287_264+288delinsCT	ENSP00000384457.1:n.264+287_264+288delinsCT
ENST00000407623.7:c.264+287_264+288delinsCT	ENSP00000384834.3:n.264+287_264+288delinsCT
ENST00000438270.1:c.264+287_264+288delinsCT	ENSP00000403439.1:n.264+287_264+288delinsCT
ENST00000470741.1:n.2467+287_2467+288delinsCT
NM_000398.6:c.333+287_333+288delinsCT	NP_000389.1:n.333+287_333+288delinsCT
NM_001129819.2:c.264+287_264+288delinsCT	NP_001123291.1:n.264+287_264+288delinsCT
NM_001171660.1:c.432+287_432+288delinsCT	NP_001165131.1:n.432+287_432+288delinsCT
NM_001171661.1:c.264+287_264+288delinsCT	NP_001165132.1:n.264+287_264+288delinsCT
NM_007326.4:c.264+287_264+288delinsCT	NP_015565.1:n.264+287_264+288delinsCT
NM_000398.7:c.333+287_333+288delinsCT MANE Select	NP_000389.1:n.333+287_333+288delinsCT
NM_001171660.2:c.432+287_432+288delinsCT	NP_001165131.1:n.432+287_432+288delinsCT