Canonical Allele Identifier: CA16040958

Gene: EVC

Linked Data

• ClinVar Variation Id: 371398
• ClinVar RCV Id: RCV000409380
• dbSNP Id: rs150814290
• MyVariant Identifiers: chr4:g.5746930G>C (hg19) ; chr4:g.5745203G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.5745203G>C , CM000666.2:g.5745203G>C	GRCh38
NC_000004.11:g.5746930G>C , CM000666.1:g.5746930G>C	GRCh37
NC_000004.10:g.5797831G>C	NCBI36
NG_008843.1:g.39007G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264956.11:c.802-1G>C MANE Select	ENSP00000264956.6:n.802-1G>C
ENST00000264956.10:c.802-1G>C	ENSP00000264956.6:n.802-1G>C
ENST00000509451.1:c.802-1G>C	ENSP00000426774.1:n.802-1G>C
NM_001306090.1:c.802-1G>C	NP_001293019.1:n.802-1G>C
NM_001306092.1:c.802-1G>C	NP_001293021.1:n.802-1G>C
NM_153717.2:c.802-1G>C	NP_714928.1:n.802-1G>C
XM_006713865.2:c.802-1G>C	XP_006713928.1:n.802-1G>C
XM_006713866.2:c.802-1G>C	XP_006713929.1:n.802-1G>C
XM_011513419.1:c.802-1G>C	XP_011511721.1:n.802-1G>C
XR_427473.2:n.992-1G>C
XR_427475.2:n.992-1G>C
XR_427476.2:n.992-1G>C
XR_924920.1:n.992-1G>C
XR_924921.1:n.992-1G>C
XR_924922.1:n.992-1G>C
XR_924923.1:n.992-1G>C
XR_924924.1:n.992-1G>C
XR_924925.1:n.992-1G>C
XR_924926.1:n.992-1G>C
XR_924927.1:n.992-1G>C
XR_924928.1:n.994-1G>C
XM_006713865.3:c.802-1G>C	XP_006713928.1:n.802-1G>C
XM_006713866.3:c.802-1G>C	XP_006713929.1:n.802-1G>C
XM_011513419.2:c.802-1G>C	XP_011511721.1:n.802-1G>C
XM_017007883.2:c.802-1G>C	XP_016863372.1:n.802-1G>C
XR_001741164.1:n.982-1G>C
XR_001741165.1:n.982-1G>C
XR_001741166.1:n.982-1G>C
XR_001741167.1:n.982-1G>C
XR_001741168.1:n.982-1G>C
XR_001741169.2:n.984-2945G>C
XR_001741170.1:n.984-1G>C
XR_001741171.1:n.287-1G>C
XR_427473.3:n.982-1G>C
XR_427475.3:n.982-1G>C
XR_427476.3:n.982-1G>C
XR_924920.2:n.982-1G>C
XR_924921.2:n.982-1G>C
XR_924922.2:n.982-1G>C
XR_924924.2:n.982-1G>C
XR_924925.2:n.982-1G>C
XR_924926.2:n.982-1G>C
NM_153717.3:c.802-1G>C MANE Select	NP_714928.1:n.802-1G>C
NM_001306090.2:c.802-1G>C	NP_001293019.1:n.802-1G>C
NM_001306092.2:c.802-1G>C	NP_001293021.1:n.802-1G>C