Canonical Allele Identifier: CA356156752

Gene: EVC

Linked Data

• gnomAD v4: 4-5711549-C-T
• MyVariant Identifiers: chr4:g.5713276C>T (hg19) ; chr4:g.5711549C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.5711549C>T , CM000666.2:g.5711549C>T	GRCh38
NC_000004.11:g.5713276C>T , CM000666.1:g.5713276C>T	GRCh37
NC_000004.10:g.5764177C>T	NCBI36
NG_008843.1:g.5353C>T
NG_015821.1:g.3000G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264956.11:c.169C>T MANE Select	ENSP00000264956.6:p.His57Tyr
ENST00000264956.10:c.169C>T	ENSP00000264956.6:p.His57Tyr
ENST00000509451.1:c.169C>T	ENSP00000426774.1:p.His57Tyr
NM_001306090.1:c.169C>T	NP_001293019.1:p.His57Tyr
NM_001306092.1:c.169C>T	NP_001293021.1:p.His57Tyr
NM_153717.2:c.169C>T	NP_714928.1:p.His57Tyr
XM_006713865.2:c.169C>T	XP_006713928.1:p.His57Tyr
XM_006713866.2:c.169C>T	XP_006713929.1:p.His57Tyr
XM_011513419.1:c.169C>T	XP_011511721.1:p.His57Tyr
XR_427473.2:n.359C>T
XR_427475.2:n.359C>T
XR_427476.2:n.359C>T
XR_924920.1:n.359C>T
XR_924921.1:n.359C>T
XR_924922.1:n.359C>T
XR_924923.1:n.359C>T
XR_924924.1:n.359C>T
XR_924925.1:n.359C>T
XR_924926.1:n.359C>T
XR_924927.1:n.359C>T
XR_924928.1:n.361C>T
XM_006713865.3:c.169C>T	XP_006713928.1:p.His57Tyr
XM_006713866.3:c.169C>T	XP_006713929.1:p.His57Tyr
XM_011513419.2:c.169C>T	XP_011511721.1:p.His57Tyr
XM_017007883.2:c.169C>T	XP_016863372.1:p.His57Tyr
XR_001741164.1:n.349C>T
XR_001741165.1:n.349C>T
XR_001741166.1:n.349C>T
XR_001741167.1:n.349C>T
XR_001741168.1:n.349C>T
XR_001741169.2:n.351C>T
XR_001741170.1:n.351C>T
XR_427473.3:n.349C>T
XR_427475.3:n.349C>T
XR_427476.3:n.349C>T
XR_924920.2:n.349C>T
XR_924921.2:n.349C>T
XR_924922.2:n.349C>T
XR_924924.2:n.349C>T
XR_924925.2:n.349C>T
XR_924926.2:n.349C>T
NM_153717.3:c.169C>T MANE Select	NP_714928.1:p.His57Tyr
NM_001306090.2:c.169C>T	NP_001293019.1:p.His57Tyr
NM_001306092.2:c.169C>T	NP_001293021.1:p.His57Tyr