Canonical Allele Identifier: CA4927810

Gene: PLEC

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143932505G>A , CM000670.2:g.143932505G>A	GRCh38
NC_000008.10:g.145006673G>A , CM000670.1:g.145006673G>A	GRCh37
NC_000008.9:g.145078661G>A	NCBI36
NG_012492.1:g.49241C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_201384.3:c.1872C>T MANE Select	NP_958786.1:p.Ala624=
ENST00000345136.8:c.1872C>T MANE Select	ENSP00000344848.3:p.Ala624=
NM_201378.4:c.1830C>T MANE Plus Clinical	NP_958780.1:p.Ala610=
ENST00000356346.7:c.1830C>T MANE Plus Clinical	ENSP00000348702.3:p.Ala610=
NM_000445.4:c.1953C>T	NP_000436.2:p.Ala651=
NM_000445.5:c.1953C>T	NP_000436.2:p.Ala651=
NM_201378.3:c.1830C>T	NP_958780.1:p.Ala610=
NM_201379.2:c.1806C>T	NP_958781.1:p.Ala602=
NM_201379.3:c.1806C>T	NP_958781.1:p.Ala602=
NM_201380.3:c.2283C>T	NP_958782.1:p.Ala761=
NM_201380.4:c.2283C>T	NP_958782.1:p.Ala761=
NM_201381.2:c.1776C>T	NP_958783.1:p.Ala592=
NM_201381.3:c.1776C>T	NP_958783.1:p.Ala592=
NM_201382.3:c.1872C>T	NP_958784.1:p.Ala624=
NM_201382.4:c.1872C>T	NP_958784.1:p.Ala624=
NM_201383.2:c.1884C>T	NP_958785.1:p.Ala628=
NM_201383.3:c.1884C>T	NP_958785.1:p.Ala628=
NM_201384.2:c.1872C>T	NP_958786.1:p.Ala624=
ENST00000322810.8:c.2283C>T	ENSP00000323856.4:p.Ala761=
ENST00000345136.7:c.1872C>T	ENSP00000344848.3:p.Ala624=
ENST00000354589.7:c.1872C>T	ENSP00000346602.3:p.Ala624=
ENST00000354958.6:c.1806C>T	ENSP00000347044.2:p.Ala602=
ENST00000357649.6:c.1884C>T	ENSP00000350277.2:p.Ala628=
ENST00000398774.6:c.1776C>T	ENSP00000381756.2:p.Ala592=
ENST00000436759.6:c.1953C>T	ENSP00000388180.2:p.Ala651=
ENST00000527096.5:c.1941C>T	ENSP00000434583.1:p.Ala647=
ENST00000527303.2:c.1953C>T	ENSP00000433982.2:p.Ala651=
ENST00000528025.5:c.2004C>T	ENSP00000437303.1:p.Ala668=
ENST00000528025.6:c.2004C>T	ENSP00000437303.2:p.Ala668=
ENST00000685198.1:c.1923C>T	ENSP00000510528.1:p.Ala641=
ENST00000687971.1:c.1590C>T	ENSP00000510788.1:p.Ala530=
ENST00000693060.1:c.1803C>T	ENSP00000510329.1:p.Ala601=
XM_005250976.2:c.2298C>T	XP_005251033.1:p.Ala766=
XM_005250976.4:c.2298C>T	XP_005251033.1:p.Ala766=
XM_005250978.2:c.1899C>T	XP_005251035.1:p.Ala633=
XM_005250978.3:c.1899C>T	XP_005251035.1:p.Ala633=
XM_005250979.3:c.1887C>T	XP_005251036.1:p.Ala629=
XM_005250979.4:c.1887C>T	XP_005251036.1:p.Ala629=
XM_005250980.3:c.1887C>T	XP_005251037.1:p.Ala629=
XM_005250980.4:c.1887C>T	XP_005251037.1:p.Ala629=
XM_005250981.2:c.1845C>T	XP_005251038.1:p.Ala615=
XM_005250981.3:c.1845C>T	XP_005251038.1:p.Ala615=
XM_005250982.2:c.1821C>T	XP_005251039.1:p.Ala607=
XM_005250982.4:c.1821C>T	XP_005251039.1:p.Ala607=
XM_005250983.2:c.1803C>T	XP_005251040.1:p.Ala601=
XM_005250984.3:c.1791C>T	XP_005251041.1:p.Ala597=
XM_005250984.5:c.1791C>T	XP_005251041.1:p.Ala597=
XM_006716588.2:c.1968C>T	XP_006716651.1:p.Ala656=
XM_006716588.3:c.1968C>T	XP_006716651.1:p.Ala656=
XM_006716589.2:c.1818C>T	XP_006716652.1:p.Ala606=
XM_006716590.2:c.1818C>T	XP_006716653.1:p.Ala606=
XM_006716590.3:c.1818C>T	XP_006716653.1:p.Ala606=
XM_011517130.1:c.1887C>T	XP_011515432.1:p.Ala629=
XM_011517130.2:c.1887C>T	XP_011515432.1:p.Ala629=
XM_011517131.1:c.1803C>T	XP_011515433.1:p.Ala601=
XM_011517131.2:c.1803C>T	XP_011515433.1:p.Ala601=
XM_011517132.1:c.1899C>T	XP_011515434.1:p.Ala633=
XM_011517132.2:c.1899C>T	XP_011515434.1:p.Ala633=