Canonical Allele Identifier: CA796573743

Gene: EVC

Linked Data

• dbSNP Id: rs1400699152
• MyVariant Identifiers: chr4:g.5713561_5713565del (hg19) ; chr4:g.5711834_5711838del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.5711835_5711839del , CM000666.2:g.5711835_5711839del	GRCh38
NC_000004.11:g.5713562_5713566del , CM000666.1:g.5713562_5713566del	GRCh37
NC_000004.10:g.5764463_5764467del	NCBI36
NG_008843.1:g.5639_5643del
NG_015821.1:g.2711_2715del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264956.11:c.174+281_174+285del MANE Select	ENSP00000264956.6:n.174+281_174+285del
ENST00000264956.10:c.174+281_174+285del	ENSP00000264956.6:n.174+281_174+285del
ENST00000509451.1:c.174+281_174+285del	ENSP00000426774.1:n.174+281_174+285del
NM_001306090.1:c.174+281_174+285del	NP_001293019.1:n.174+281_174+285del
NM_001306092.1:c.174+281_174+285del	NP_001293021.1:n.174+281_174+285del
NM_153717.2:c.174+281_174+285del	NP_714928.1:n.174+281_174+285del
XM_006713865.2:c.174+281_174+285del	XP_006713928.1:n.174+281_174+285del
XM_006713866.2:c.174+281_174+285del	XP_006713929.1:n.174+281_174+285del
XM_011513419.1:c.174+281_174+285del	XP_011511721.1:n.174+281_174+285del
XR_427473.2:n.364+281_364+285del
XR_427475.2:n.364+281_364+285del
XR_427476.2:n.364+281_364+285del
XR_924920.1:n.364+281_364+285del
XR_924921.1:n.364+281_364+285del
XR_924922.1:n.364+281_364+285del
XR_924923.1:n.364+281_364+285del
XR_924924.1:n.364+281_364+285del
XR_924925.1:n.364+281_364+285del
XR_924926.1:n.364+281_364+285del
XR_924927.1:n.364+281_364+285del
XR_924928.1:n.366+281_366+285del
XM_006713865.3:c.174+281_174+285del	XP_006713928.1:n.174+281_174+285del
XM_006713866.3:c.174+281_174+285del	XP_006713929.1:n.174+281_174+285del
XM_011513419.2:c.174+281_174+285del	XP_011511721.1:n.174+281_174+285del
XM_017007883.2:c.174+281_174+285del	XP_016863372.1:n.174+281_174+285del
XR_001741164.1:n.354+281_354+285del
XR_001741165.1:n.354+281_354+285del
XR_001741166.1:n.354+281_354+285del
XR_001741167.1:n.354+281_354+285del
XR_001741168.1:n.354+281_354+285del
XR_001741169.2:n.356+281_356+285del
XR_001741170.1:n.356+281_356+285del
XR_427473.3:n.354+281_354+285del
XR_427475.3:n.354+281_354+285del
XR_427476.3:n.354+281_354+285del
XR_924920.2:n.354+281_354+285del
XR_924921.2:n.354+281_354+285del
XR_924922.2:n.354+281_354+285del
XR_924924.2:n.354+281_354+285del
XR_924925.2:n.354+281_354+285del
XR_924926.2:n.354+281_354+285del
NM_153717.3:c.174+281_174+285del MANE Select	NP_714928.1:n.174+281_174+285del
NM_001306090.2:c.174+281_174+285del	NP_001293019.1:n.174+281_174+285del
NM_001306092.2:c.174+281_174+285del	NP_001293021.1:n.174+281_174+285del