Canonical Allele Identifier: CA1619278971
Gene: MPIG6B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31723908C= , CM000668.2:g.31723908C= GRCh38
NC_000006.11:g.31691685C= , CM000668.1:g.31691685C= GRCh37
NC_000006.10:g.31799664C= NCBI36
NG_029044.1:g.5565C=
NG_029044.2:g.5565C=

Transcript Alleles

HGVS Amino-acid change
ENST00000649779.1:c.331C= MANE Select ENSP00000497720.1:p.Arg111=
ENST00000375804.6:c.331C= ENSP00000364962.2:p.Arg111=
ENST00000375805.6:c.331C= ENSP00000364963.2:p.Arg111=
ENST00000375806.2:c.331C= ENSP00000364964.2:p.Arg111=
ENST00000375809.7:c.331C= ENSP00000364967.3:p.Arg111=
ENST00000375810.8:c.331C= ENSP00000364968.4:p.Arg111=
ENST00000375814.7:c.331C= ENSP00000364972.3:p.Arg111=
ENST00000460663.5:n.538C=
ENST00000466312.5:n.335C=
ENST00000471545.1:n.331C=
ENST00000480039.5:c.331C= ENSP00000419306.1:p.Arg111=
ENST00000485548.5:c.268+63C= ENSP00000420355.1:n.268+63C=
NM_025260.3:c.331C= NP_079536.2:p.Arg111=
NM_138272.2:c.331C= NP_612116.1:p.Arg111=
NM_138273.2:c.331C= NP_612117.1:p.Arg111=
NM_138274.2:c.331C= NP_612118.1:p.Arg111=
NM_138275.2:c.331C= NP_612119.1:p.Arg111=
NM_138277.2:c.331C= NP_612121.1:p.Arg111=
XM_011514920.1:c.379C= XP_011513222.1:p.Arg127=
XM_011514921.1:c.379C= XP_011513223.1:p.Arg127=
XM_011514920.2:c.379C= XP_011513222.1:p.Arg127=
XM_011514921.2:c.379C= XP_011513223.1:p.Arg127=
XM_017011330.1:c.379C= XP_016866819.1:p.Arg127=
XM_017011331.1:c.331C= XP_016866820.1:p.Arg111=
XM_017011332.1:c.379C= XP_016866821.1:p.Arg127=
XM_017011333.1:c.379C= XP_016866822.1:p.Arg127=
NM_025260.4:c.331C= NP_079536.2:p.Arg111=
NM_138272.3:c.331C= MANE Select NP_612116.1:p.Arg111=
NM_138273.3:c.331C= NP_612117.1:p.Arg111=
NM_138274.3:c.331C= NP_612118.1:p.Arg111=
NM_138275.3:c.331C= NP_612119.1:p.Arg111=
NM_138277.3:c.331C= NP_612121.1:p.Arg111=