Canonical Allele Identifier: CA2669805844

Gene: EVC

Linked Data

• gnomAD v4: 4-5711232-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.5711233del , CM000666.2:g.5711233del	GRCh38
NC_000004.11:g.5712960del , CM000666.1:g.5712960del	GRCh37
NC_000004.10:g.5763861del	NCBI36
NG_008843.1:g.5037del
NG_015821.1:g.3316del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264956.11:c.-148del MANE Select	ENSP00000264956.6:n.-148del
ENST00000264956.10:c.-148del	ENSP00000264956.6:n.-148del
ENST00000509451.1:c.-148del	ENSP00000426774.1:n.-148del
NM_001306090.1:c.-148del	NP_001293019.1:n.-148del
NM_001306092.1:c.-148del	NP_001293021.1:n.-148del
NM_153717.2:c.-148del	NP_714928.1:n.-148del
XM_006713865.2:c.-148del	XP_006713928.1:n.-148del
XM_006713866.2:c.-148del	XP_006713929.1:n.-148del
XM_011513419.1:c.-148del	XP_011511721.1:n.-148del
XR_427473.2:n.43del
XR_427475.2:n.43del
XR_427476.2:n.43del
XR_924920.1:n.43del
XR_924921.1:n.43del
XR_924922.1:n.43del
XR_924923.1:n.43del
XR_924924.1:n.43del
XR_924925.1:n.43del
XR_924926.1:n.43del
XR_924927.1:n.43del
XR_924928.1:n.45del
XM_006713865.3:c.-148del	XP_006713928.1:n.-148del
XM_006713866.3:c.-148del	XP_006713929.1:n.-148del
XM_011513419.2:c.-148del	XP_011511721.1:n.-148del
XM_017007883.2:c.-148del	XP_016863372.1:n.-148del
XR_001741164.1:n.33del
XR_001741165.1:n.33del
XR_001741166.1:n.33del
XR_001741167.1:n.33del
XR_001741168.1:n.33del
XR_001741169.2:n.35del
XR_001741170.1:n.35del
XR_427473.3:n.33del
XR_427475.3:n.33del
XR_427476.3:n.33del
XR_924920.2:n.33del
XR_924921.2:n.33del
XR_924922.2:n.33del
XR_924924.2:n.33del
XR_924925.2:n.33del
XR_924926.2:n.33del
NM_153717.3:c.-148del MANE Select	NP_714928.1:n.-148del
NM_001306090.2:c.-148del	NP_001293019.1:n.-148del
NM_001306092.2:c.-148del	NP_001293021.1:n.-148del