Canonical Allele Identifier: CA1435469800

Gene: EVC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.5711853_5711854delinsAG , CM000666.2:g.5711853_5711854delinsAG	GRCh38
NC_000004.11:g.5713580_5713581delinsAG , CM000666.1:g.5713580_5713581delinsAG	GRCh37
NC_000004.10:g.5764481_5764482delinsAG	NCBI36
NG_008843.1:g.5657_5658delinsAG
NG_015821.1:g.2695_2696delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264956.11:c.174+299_174+300delinsAG MANE Select	ENSP00000264956.6:n.174+299_174+300delinsAG
ENST00000264956.10:c.174+299_174+300delinsAG	ENSP00000264956.6:n.174+299_174+300delinsAG
ENST00000509451.1:c.174+299_174+300delinsAG	ENSP00000426774.1:n.174+299_174+300delinsAG
NM_001306090.1:c.174+299_174+300delinsAG	NP_001293019.1:n.174+299_174+300delinsAG
NM_001306092.1:c.174+299_174+300delinsAG	NP_001293021.1:n.174+299_174+300delinsAG
NM_153717.2:c.174+299_174+300delinsAG	NP_714928.1:n.174+299_174+300delinsAG
XM_006713865.2:c.174+299_174+300delinsAG	XP_006713928.1:n.174+299_174+300delinsAG
XM_006713866.2:c.174+299_174+300delinsAG	XP_006713929.1:n.174+299_174+300delinsAG
XM_011513419.1:c.174+299_174+300delinsAG	XP_011511721.1:n.174+299_174+300delinsAG
XR_427473.2:n.364+299_364+300delinsAG
XR_427475.2:n.364+299_364+300delinsAG
XR_427476.2:n.364+299_364+300delinsAG
XR_924920.1:n.364+299_364+300delinsAG
XR_924921.1:n.364+299_364+300delinsAG
XR_924922.1:n.364+299_364+300delinsAG
XR_924923.1:n.364+299_364+300delinsAG
XR_924924.1:n.364+299_364+300delinsAG
XR_924925.1:n.364+299_364+300delinsAG
XR_924926.1:n.364+299_364+300delinsAG
XR_924927.1:n.364+299_364+300delinsAG
XR_924928.1:n.366+299_366+300delinsAG
XM_006713865.3:c.174+299_174+300delinsAG	XP_006713928.1:n.174+299_174+300delinsAG
XM_006713866.3:c.174+299_174+300delinsAG	XP_006713929.1:n.174+299_174+300delinsAG
XM_011513419.2:c.174+299_174+300delinsAG	XP_011511721.1:n.174+299_174+300delinsAG
XM_017007883.2:c.174+299_174+300delinsAG	XP_016863372.1:n.174+299_174+300delinsAG
XR_001741164.1:n.354+299_354+300delinsAG
XR_001741165.1:n.354+299_354+300delinsAG
XR_001741166.1:n.354+299_354+300delinsAG
XR_001741167.1:n.354+299_354+300delinsAG
XR_001741168.1:n.354+299_354+300delinsAG
XR_001741169.2:n.356+299_356+300delinsAG
XR_001741170.1:n.356+299_356+300delinsAG
XR_427473.3:n.354+299_354+300delinsAG
XR_427475.3:n.354+299_354+300delinsAG
XR_427476.3:n.354+299_354+300delinsAG
XR_924920.2:n.354+299_354+300delinsAG
XR_924921.2:n.354+299_354+300delinsAG
XR_924922.2:n.354+299_354+300delinsAG
XR_924924.2:n.354+299_354+300delinsAG
XR_924925.2:n.354+299_354+300delinsAG
XR_924926.2:n.354+299_354+300delinsAG
NM_153717.3:c.174+299_174+300delinsAG MANE Select	NP_714928.1:n.174+299_174+300delinsAG
NM_001306090.2:c.174+299_174+300delinsAG	NP_001293019.1:n.174+299_174+300delinsAG
NM_001306092.2:c.174+299_174+300delinsAG	NP_001293021.1:n.174+299_174+300delinsAG