Canonical Allele Identifier: CA2657075110

Gene: CYB5R3

Linked Data

• gnomAD v4: 22-42623754-TCCCA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42623763_42623766del , CM000684.2:g.42623763_42623766del	GRCh38
NC_000022.10:g.43019769_43019772del , CM000684.1:g.43019769_43019772del	GRCh37
NC_000022.9:g.41349713_41349716del	NCBI36
NG_012194.1:g.30642_30645del

Transcript Alleles

HGVS	Amino-acid change
ENST00000361740.9:c.865+31_865+34del	ENSP00000354468.5:n.865+31_865+34del
ENST00000402438.6:c.664+31_664+34del	ENSP00000385679.1:n.664+31_664+34del
ENST00000407332.6:c.751+31_751+34del	ENSP00000384457.2:n.751+31_751+34del
ENST00000407623.8:c.664+31_664+34del	ENSP00000384834.3:n.664+31_664+34del
ENST00000617178.5:c.270+31_270+34del
ENST00000684963.1:n.2473+31_2473+34del
ENST00000685184.1:n.325+31_325+34del
ENST00000686523.1:c.*682+31_*682+34del	ENSP00000508940.1:n.*682+31_*682+34del
ENST00000687183.1:n.1009+31_1009+34del
ENST00000687198.1:c.664+31_664+34del	ENSP00000508492.1:n.664+31_664+34del
ENST00000688117.1:c.832+31_832+34del	ENSP00000509015.1:n.832+31_832+34del
ENST00000688244.1:c.433+31_433+34del	ENSP00000510355.1:n.433+31_433+34del
ENST00000689001.1:n.1355+31_1355+34del
ENST00000689195.1:c.649+31_649+34del	ENSP00000509895.1:n.649+31_649+34del
ENST00000689239.1:n.900+31_900+34del
ENST00000689795.1:n.994+31_994+34del
ENST00000690835.1:c.*112+31_*112+34del	ENSP00000509038.1:n.*112+31_*112+34del
ENST00000690993.1:n.1488+31_1488+34del
ENST00000691295.1:c.*216+31_*216+34del	ENSP00000508706.1:n.*216+31_*216+34del
ENST00000692152.1:c.664+31_664+34del	ENSP00000509317.1:n.664+31_664+34del
ENST00000692344.1:n.1220+31_1220+34del
ENST00000693363.1:c.775+31_775+34del	ENSP00000510411.1:n.775+31_775+34del
ENST00000693367.1:c.733+31_733+34del	ENSP00000508815.1:n.733+31_733+34del
ENST00000352397.10:c.733+31_733+34del MANE Select	ENSP00000338461.6:n.733+31_733+34del
ENST00000352397.9:c.733+31_733+34del	ENSP00000338461.6:n.733+31_733+34del
ENST00000361740.8:c.832+31_832+34del	ENSP00000354468.4:n.832+31_832+34del
ENST00000402438.5:c.664+31_664+34del	ENSP00000385679.1:n.664+31_664+34del
ENST00000407332.5:c.664+31_664+34del	ENSP00000384457.1:n.664+31_664+34del
ENST00000407623.7:c.664+31_664+34del	ENSP00000384834.3:n.664+31_664+34del
ENST00000470741.1:n.2867+31_2867+34del
NM_000398.6:c.733+31_733+34del	NP_000389.1:n.733+31_733+34del
NM_001129819.2:c.664+31_664+34del	NP_001123291.1:n.664+31_664+34del
NM_001171660.1:c.832+31_832+34del	NP_001165131.1:n.832+31_832+34del
NM_001171661.1:c.664+31_664+34del	NP_001165132.1:n.664+31_664+34del
NM_007326.4:c.664+31_664+34del	NP_015565.1:n.664+31_664+34del
NM_000398.7:c.733+31_733+34del MANE Select	NP_000389.1:n.733+31_733+34del
NM_001171660.2:c.832+31_832+34del	NP_001165131.1:n.832+31_832+34del