Canonical Allele Identifier: CA438206326

Gene: EVC

Linked Data

• ClinVar Variation Id: 1528648
• ClinVar RCV Id: RCV002077585
• dbSNP Id: rs1479357518
• gnomAD v2: 4-5713146-G-A
• gnomAD v4: 4-5711419-G-A
• MyVariant Identifiers: chr4:g.5713146G>A (hg19) ; chr4:g.5711419G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.5711419G>A , CM000666.2:g.5711419G>A	GRCh38
NC_000004.11:g.5713146G>A , CM000666.1:g.5713146G>A	GRCh37
NC_000004.10:g.5764047G>A	NCBI36
NG_008843.1:g.5223G>A
NG_015821.1:g.3130C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264956.11:c.39G>A MANE Select	ENSP00000264956.6:p.Arg13=
ENST00000264956.10:c.39G>A	ENSP00000264956.6:p.Arg13=
ENST00000509451.1:c.39G>A	ENSP00000426774.1:p.Arg13=
NM_001306090.1:c.39G>A	NP_001293019.1:p.Arg13=
NM_001306092.1:c.39G>A	NP_001293021.1:p.Arg13=
NM_153717.2:c.39G>A	NP_714928.1:p.Arg13=
XM_006713865.2:c.39G>A	XP_006713928.1:p.Arg13=
XM_006713866.2:c.39G>A	XP_006713929.1:p.Arg13=
XM_011513419.1:c.39G>A	XP_011511721.1:p.Arg13=
XR_427473.2:n.229G>A
XR_427475.2:n.229G>A
XR_427476.2:n.229G>A
XR_924920.1:n.229G>A
XR_924921.1:n.229G>A
XR_924922.1:n.229G>A
XR_924923.1:n.229G>A
XR_924924.1:n.229G>A
XR_924925.1:n.229G>A
XR_924926.1:n.229G>A
XR_924927.1:n.229G>A
XR_924928.1:n.231G>A
XM_006713865.3:c.39G>A	XP_006713928.1:p.Arg13=
XM_006713866.3:c.39G>A	XP_006713929.1:p.Arg13=
XM_011513419.2:c.39G>A	XP_011511721.1:p.Arg13=
XM_017007883.2:c.39G>A	XP_016863372.1:p.Arg13=
XR_001741164.1:n.219G>A
XR_001741165.1:n.219G>A
XR_001741166.1:n.219G>A
XR_001741167.1:n.219G>A
XR_001741168.1:n.219G>A
XR_001741169.2:n.221G>A
XR_001741170.1:n.221G>A
XR_427473.3:n.219G>A
XR_427475.3:n.219G>A
XR_427476.3:n.219G>A
XR_924920.2:n.219G>A
XR_924921.2:n.219G>A
XR_924922.2:n.219G>A
XR_924924.2:n.219G>A
XR_924925.2:n.219G>A
XR_924926.2:n.219G>A
NM_153717.3:c.39G>A MANE Select	NP_714928.1:p.Arg13=
NM_001306090.2:c.39G>A	NP_001293019.1:p.Arg13=
NM_001306092.2:c.39G>A	NP_001293021.1:p.Arg13=