Canonical Allele Identifier: CA356147772

Gene: EVC2

Linked Data

• MyVariant Identifiers: chr4:g.5630400C>G (hg19) ; chr4:g.5628673C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.5628673C>G , CM000666.2:g.5628673C>G	GRCh38
NC_000004.11:g.5630400C>G , CM000666.1:g.5630400C>G	GRCh37
NC_000004.10:g.5681301C>G	NCBI36
NG_015821.1:g.85876G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344408.10:c.1772G>C MANE Select	ENSP00000342144.5:p.Arg591Thr
ENST00000310917.6:c.1532G>C	ENSP00000311683.2:p.Arg511Thr
ENST00000344408.9:c.1772G>C	ENSP00000342144.5:p.Arg591Thr
ENST00000475313.5:c.1532G>C	ENSP00000431981.1:p.Arg511Thr
ENST00000509670.1:c.*165G>C	ENSP00000423876.1:n.*165G>C
NM_001166136.1:c.1532G>C	NP_001159608.1:p.Arg511Thr
NM_147127.4:c.1772G>C	NP_667338.3:p.Arg591Thr
XM_011513392.1:c.1781G>C	XP_011511694.1:p.Arg594Thr
XM_011513393.1:c.1781G>C	XP_011511695.1:p.Arg594Thr
XM_011513394.1:c.1541G>C	XP_011511696.1:p.Arg514Thr
XM_017007736.1:c.1532G>C	XP_016863225.1:p.Arg511Thr
XM_017007737.1:c.1532G>C	XP_016863226.1:p.Arg511Thr
XM_017007738.1:c.1772G>C	XP_016863227.1:p.Arg591Thr
XM_017007739.1:c.92G>C	XP_016863228.1:p.Arg31Thr
XM_024453893.1:c.92G>C	XP_024309661.1:p.Arg31Thr
XR_001741141.1:n.1837G>C
NM_147127.5:c.1772G>C MANE Select	NP_667338.3:p.Arg591Thr
NM_001166136.2:c.1532G>C	NP_001159608.1:p.Arg511Thr