Canonical Allele Identifier: CA356147644

Gene: EVC2

Linked Data

• MyVariant Identifiers: chr4:g.5630359A>G (hg19) ; chr4:g.5628632A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.5628632A>G , CM000666.2:g.5628632A>G	GRCh38
NC_000004.11:g.5630359A>G , CM000666.1:g.5630359A>G	GRCh37
NC_000004.10:g.5681260A>G	NCBI36
NG_015821.1:g.85917T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344408.10:c.1813T>C MANE Select	ENSP00000342144.5:p.Ser605Pro
ENST00000310917.6:c.1573T>C	ENSP00000311683.2:p.Ser525Pro
ENST00000344408.9:c.1813T>C	ENSP00000342144.5:p.Ser605Pro
ENST00000475313.5:c.1573T>C	ENSP00000431981.1:p.Ser525Pro
ENST00000509670.1:c.*206T>C	ENSP00000423876.1:n.*206T>C
NM_001166136.1:c.1573T>C	NP_001159608.1:p.Ser525Pro
NM_147127.4:c.1813T>C	NP_667338.3:p.Ser605Pro
XM_011513392.1:c.1822T>C	XP_011511694.1:p.Ser608Pro
XM_011513393.1:c.1822T>C	XP_011511695.1:p.Ser608Pro
XM_011513394.1:c.1582T>C	XP_011511696.1:p.Ser528Pro
XM_017007736.1:c.1573T>C	XP_016863225.1:p.Ser525Pro
XM_017007737.1:c.1573T>C	XP_016863226.1:p.Ser525Pro
XM_017007738.1:c.1813T>C	XP_016863227.1:p.Ser605Pro
XM_017007739.1:c.133T>C	XP_016863228.1:p.Ser45Pro
XM_024453893.1:c.133T>C	XP_024309661.1:p.Ser45Pro
XR_001741141.1:n.1878T>C
NM_147127.5:c.1813T>C MANE Select	NP_667338.3:p.Ser605Pro
NM_001166136.2:c.1573T>C	NP_001159608.1:p.Ser525Pro