Canonical Allele Identifier: CA438206447

Gene: EVC

Linked Data

• ClinVar Variation Id: 1119127
• ClinVar RCV Id: RCV001448495
• dbSNP Id: rs2151767494
• gnomAD v4: 4-5711461-G-T
• MyVariant Identifiers: chr4:g.5713188G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.5711461G>T , CM000666.2:g.5711461G>T	GRCh38
NC_000004.11:g.5713188G>T , CM000666.1:g.5713188G>T	GRCh37
NC_000004.10:g.5764089G>T	NCBI36
NG_008843.1:g.5265G>T
NG_015821.1:g.3088C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000264956.11:c.81G>T MANE Select	ENSP00000264956.6:p.Leu27=
ENST00000264956.10:c.81G>T	ENSP00000264956.6:p.Leu27=
ENST00000509451.1:c.81G>T	ENSP00000426774.1:p.Leu27=
NM_001306090.1:c.81G>T	NP_001293019.1:p.Leu27=
NM_001306092.1:c.81G>T	NP_001293021.1:p.Leu27=
NM_153717.2:c.81G>T	NP_714928.1:p.Leu27=
XM_006713865.2:c.81G>T	XP_006713928.1:p.Leu27=
XM_006713866.2:c.81G>T	XP_006713929.1:p.Leu27=
XM_011513419.1:c.81G>T	XP_011511721.1:p.Leu27=
XR_427473.2:n.271G>T
XR_427475.2:n.271G>T
XR_427476.2:n.271G>T
XR_924920.1:n.271G>T
XR_924921.1:n.271G>T
XR_924922.1:n.271G>T
XR_924923.1:n.271G>T
XR_924924.1:n.271G>T
XR_924925.1:n.271G>T
XR_924926.1:n.271G>T
XR_924927.1:n.271G>T
XR_924928.1:n.273G>T
XM_006713865.3:c.81G>T	XP_006713928.1:p.Leu27=
XM_006713866.3:c.81G>T	XP_006713929.1:p.Leu27=
XM_011513419.2:c.81G>T	XP_011511721.1:p.Leu27=
XM_017007883.2:c.81G>T	XP_016863372.1:p.Leu27=
XR_001741164.1:n.261G>T
XR_001741165.1:n.261G>T
XR_001741166.1:n.261G>T
XR_001741167.1:n.261G>T
XR_001741168.1:n.261G>T
XR_001741169.2:n.263G>T
XR_001741170.1:n.263G>T
XR_427473.3:n.261G>T
XR_427475.3:n.261G>T
XR_427476.3:n.261G>T
XR_924920.2:n.261G>T
XR_924921.2:n.261G>T
XR_924922.2:n.261G>T
XR_924924.2:n.261G>T
XR_924925.2:n.261G>T
XR_924926.2:n.261G>T
NM_153717.3:c.81G>T MANE Select	NP_714928.1:p.Leu27=
NM_001306090.2:c.81G>T	NP_001293019.1:p.Leu27=
NM_001306092.2:c.81G>T	NP_001293021.1:p.Leu27=