Canonical Allele Identifier: CA2669805984

Gene: EVC

Linked Data

• gnomAD v4: 4-5711346-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.5711349del , CM000666.2:g.5711349del	GRCh38
NC_000004.11:g.5713076del , CM000666.1:g.5713076del	GRCh37
NC_000004.10:g.5763977del	NCBI36
NG_008843.1:g.5153del
NG_015821.1:g.3202del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264956.11:c.-32del MANE Select	ENSP00000264956.6:n.-32del
ENST00000264956.10:c.-32del	ENSP00000264956.6:n.-32del
ENST00000509451.1:c.-32del	ENSP00000426774.1:n.-32del
NM_001306090.1:c.-32del	NP_001293019.1:n.-32del
NM_001306092.1:c.-32del	NP_001293021.1:n.-32del
NM_153717.2:c.-32del	NP_714928.1:n.-32del
XM_006713865.2:c.-32del	XP_006713928.1:n.-32del
XM_006713866.2:c.-32del	XP_006713929.1:n.-32del
XM_011513419.1:c.-32del	XP_011511721.1:n.-32del
XR_427473.2:n.159del
XR_427475.2:n.159del
XR_427476.2:n.159del
XR_924920.1:n.159del
XR_924921.1:n.159del
XR_924922.1:n.159del
XR_924923.1:n.159del
XR_924924.1:n.159del
XR_924925.1:n.159del
XR_924926.1:n.159del
XR_924927.1:n.159del
XR_924928.1:n.161del
XM_006713865.3:c.-32del	XP_006713928.1:n.-32del
XM_006713866.3:c.-32del	XP_006713929.1:n.-32del
XM_011513419.2:c.-32del	XP_011511721.1:n.-32del
XM_017007883.2:c.-32del	XP_016863372.1:n.-32del
XR_001741164.1:n.149del
XR_001741165.1:n.149del
XR_001741166.1:n.149del
XR_001741167.1:n.149del
XR_001741168.1:n.149del
XR_001741169.2:n.151del
XR_001741170.1:n.151del
XR_427473.3:n.149del
XR_427475.3:n.149del
XR_427476.3:n.149del
XR_924920.2:n.149del
XR_924921.2:n.149del
XR_924922.2:n.149del
XR_924924.2:n.149del
XR_924925.2:n.149del
XR_924926.2:n.149del
NM_153717.3:c.-32del MANE Select	NP_714928.1:n.-32del
NM_001306090.2:c.-32del	NP_001293019.1:n.-32del
NM_001306092.2:c.-32del	NP_001293021.1:n.-32del