Canonical Allele Identifier: CA1087473094

Gene: MPIG6B

Linked Data

• gnomAD v3: 6-31723909-G-GCCACGAGGACGAGAGCCGTACAGTGCTTCACGTGCTGGGGGACAGGACCTATTGCAAGGCCCC
• gnomAD v4: 6-31723909-G-GCCACGAGGACGAGAGCCGTACAGTGCTTCACGTGCTGGGGGACAGGACCTATTGCAAGGCCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31723911_31723973dup , CM000668.2:g.31723911_31723973dup	GRCh38
NC_000006.11:g.31691688_31691750dup , CM000668.1:g.31691688_31691750dup	GRCh37
NC_000006.10:g.31799667_31799729dup	NCBI36
NG_029044.1:g.5568_5630dup
NG_029044.2:g.5568_5630dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000649779.1:c.334_396dup MANE Select	ENSP00000497720.1:p.Pro132_Gly133insHisGl...
ENST00000375804.6:c.334_396dup	ENSP00000364962.2:p.Pro132_Gly133insHisGl...
ENST00000375805.6:c.334_396dup	ENSP00000364963.2:p.Pro132_Gly133insHisGl...
ENST00000375806.2:c.334_396dup	ENSP00000364964.2:p.Pro132_Gly133insHisGl...
ENST00000375809.7:c.334_396dup	ENSP00000364967.3:p.Pro132_Gly133insHisGl...
ENST00000375810.8:c.334_396dup	ENSP00000364968.4:p.Pro132_Gly133insHisGl...
ENST00000375814.7:c.334_396dup	ENSP00000364972.3:p.Pro132_Gly133insHisGl...
ENST00000460663.5:n.541_603dup
ENST00000466312.5:n.338_400dup
ENST00000471545.1:n.334_396dup
ENST00000480039.5:c.334_396dup	ENSP00000419306.1:p.Pro132_Gly133insHisGl...
ENST00000485548.5:c.268+66_268+128dup	ENSP00000420355.1:n.268+66_268+128dup
NM_025260.3:c.334_396dup	NP_079536.2:p.Pro132_Gly133insHisGluAspGl...
NM_138272.2:c.334_396dup	NP_612116.1:p.Pro132_Gly133insHisGluAspGl...
NM_138273.2:c.334_396dup	NP_612117.1:p.Pro132_Gly133insHisGluAspGl...
NM_138274.2:c.334_396dup	NP_612118.1:p.Pro132_Gly133insHisGluAspGl...
NM_138275.2:c.334_396dup	NP_612119.1:p.Pro132_Gly133insHisGluAspGl...
NM_138277.2:c.334_396dup	NP_612121.1:p.Pro132_Gly133insHisGluAspGl...
XM_011514920.1:c.382_444dup	XP_011513222.1:p.Pro148_Gly149insHisGluAs...
XM_011514921.1:c.382_444dup	XP_011513223.1:p.Pro148_Gly149insHisGluAs...
XM_011514920.2:c.382_444dup	XP_011513222.1:p.Pro148_Gly149insHisGluAs...
XM_011514921.2:c.382_444dup	XP_011513223.1:p.Pro148_Gly149insHisGluAs...
XM_017011330.1:c.382_444dup	XP_016866819.1:p.Pro148_Gly149insHisGluAs...
XM_017011331.1:c.334_396dup	XP_016866820.1:p.Pro132_Gly133insHisGluAs...
XM_017011332.1:c.382_444dup	XP_016866821.1:p.Pro148_Gly149insHisGluAs...
XM_017011333.1:c.382_444dup	XP_016866822.1:p.Pro148_Gly149insHisGluAs...
NM_025260.4:c.334_396dup	NP_079536.2:p.Pro132_Gly133insHisGluAspGl...
NM_138272.3:c.334_396dup MANE Select	NP_612116.1:p.Pro132_Gly133insHisGluAspGl...
NM_138273.3:c.334_396dup	NP_612117.1:p.Pro132_Gly133insHisGluAspGl...
NM_138274.3:c.334_396dup	NP_612118.1:p.Pro132_Gly133insHisGluAspGl...
NM_138275.3:c.334_396dup	NP_612119.1:p.Pro132_Gly133insHisGluAspGl...
NM_138277.3:c.334_396dup	NP_612121.1:p.Pro132_Gly133insHisGluAspGl...