Canonical Allele Identifier: CA438206421

Gene: EVC

Linked Data

• ClinVar Variation Id: 2040992
• ClinVar RCV Id: RCV002890891
• gnomAD v4: 4-5711452-G-C
• MyVariant Identifiers: chr4:g.5713179G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.5711452G>C , CM000666.2:g.5711452G>C	GRCh38
NC_000004.11:g.5713179G>C , CM000666.1:g.5713179G>C	GRCh37
NC_000004.10:g.5764080G>C	NCBI36
NG_008843.1:g.5256G>C
NG_015821.1:g.3097C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000264956.11:c.72G>C MANE Select	ENSP00000264956.6:p.Ala24=
ENST00000264956.10:c.72G>C	ENSP00000264956.6:p.Ala24=
ENST00000509451.1:c.72G>C	ENSP00000426774.1:p.Ala24=
NM_001306090.1:c.72G>C	NP_001293019.1:p.Ala24=
NM_001306092.1:c.72G>C	NP_001293021.1:p.Ala24=
NM_153717.2:c.72G>C	NP_714928.1:p.Ala24=
XM_006713865.2:c.72G>C	XP_006713928.1:p.Ala24=
XM_006713866.2:c.72G>C	XP_006713929.1:p.Ala24=
XM_011513419.1:c.72G>C	XP_011511721.1:p.Ala24=
XR_427473.2:n.262G>C
XR_427475.2:n.262G>C
XR_427476.2:n.262G>C
XR_924920.1:n.262G>C
XR_924921.1:n.262G>C
XR_924922.1:n.262G>C
XR_924923.1:n.262G>C
XR_924924.1:n.262G>C
XR_924925.1:n.262G>C
XR_924926.1:n.262G>C
XR_924927.1:n.262G>C
XR_924928.1:n.264G>C
XM_006713865.3:c.72G>C	XP_006713928.1:p.Ala24=
XM_006713866.3:c.72G>C	XP_006713929.1:p.Ala24=
XM_011513419.2:c.72G>C	XP_011511721.1:p.Ala24=
XM_017007883.2:c.72G>C	XP_016863372.1:p.Ala24=
XR_001741164.1:n.252G>C
XR_001741165.1:n.252G>C
XR_001741166.1:n.252G>C
XR_001741167.1:n.252G>C
XR_001741168.1:n.252G>C
XR_001741169.2:n.254G>C
XR_001741170.1:n.254G>C
XR_427473.3:n.252G>C
XR_427475.3:n.252G>C
XR_427476.3:n.252G>C
XR_924920.2:n.252G>C
XR_924921.2:n.252G>C
XR_924922.2:n.252G>C
XR_924924.2:n.252G>C
XR_924925.2:n.252G>C
XR_924926.2:n.252G>C
NM_153717.3:c.72G>C MANE Select	NP_714928.1:p.Ala24=
NM_001306090.2:c.72G>C	NP_001293019.1:p.Ala24=
NM_001306092.2:c.72G>C	NP_001293021.1:p.Ala24=