Canonical Allele Identifier: CA2678022770

Gene: MPIG6B

Linked Data

• gnomAD v4: 6-31724041-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31724041A>C , CM000668.2:g.31724041A>C	GRCh38
NC_000006.11:g.31691818A>C , CM000668.1:g.31691818A>C	GRCh37
NC_000006.10:g.31799797A>C	NCBI36
NG_029044.1:g.5698A>C
NG_029044.2:g.5698A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649779.1:c.409+55A>C MANE Select	ENSP00000497720.1:n.409+55A>C
ENST00000375804.6:c.409+55A>C	ENSP00000364962.2:n.409+55A>C
ENST00000375805.6:c.409+55A>C	ENSP00000364963.2:n.409+55A>C
ENST00000375806.2:c.409+55A>C	ENSP00000364964.2:n.409+55A>C
ENST00000375809.7:c.409+55A>C	ENSP00000364967.3:n.409+55A>C
ENST00000375810.8:c.409+55A>C	ENSP00000364968.4:n.409+55A>C
ENST00000375814.7:c.409+55A>C	ENSP00000364972.3:n.409+55A>C
ENST00000460663.5:n.616+55A>C
ENST00000466312.5:n.413+55A>C
ENST00000471545.1:n.409+55A>C
ENST00000480039.5:c.409+55A>C	ENSP00000419306.1:n.409+55A>C
ENST00000485548.5:c.269-118A>C	ENSP00000420355.1:n.269-118A>C
NM_025260.3:c.409+55A>C	NP_079536.2:n.409+55A>C
NM_138272.2:c.409+55A>C	NP_612116.1:n.409+55A>C
NM_138273.2:c.409+55A>C	NP_612117.1:n.409+55A>C
NM_138274.2:c.409+55A>C	NP_612118.1:n.409+55A>C
NM_138275.2:c.409+55A>C	NP_612119.1:n.409+55A>C
NM_138277.2:c.409+55A>C	NP_612121.1:n.409+55A>C
XM_011514920.1:c.457+55A>C	XP_011513222.1:n.457+55A>C
XM_011514921.1:c.457+55A>C	XP_011513223.1:n.457+55A>C
XM_011514920.2:c.457+55A>C	XP_011513222.1:n.457+55A>C
XM_011514921.2:c.457+55A>C	XP_011513223.1:n.457+55A>C
XM_017011330.1:c.457+55A>C	XP_016866819.1:n.457+55A>C
XM_017011331.1:c.409+55A>C	XP_016866820.1:n.409+55A>C
XM_017011332.1:c.457+55A>C	XP_016866821.1:n.457+55A>C
XM_017011333.1:c.457+55A>C	XP_016866822.1:n.457+55A>C
NM_025260.4:c.409+55A>C	NP_079536.2:n.409+55A>C
NM_138272.3:c.409+55A>C MANE Select	NP_612116.1:n.409+55A>C
NM_138273.3:c.409+55A>C	NP_612117.1:n.409+55A>C
NM_138274.3:c.409+55A>C	NP_612118.1:n.409+55A>C
NM_138275.3:c.409+55A>C	NP_612119.1:n.409+55A>C
NM_138277.3:c.409+55A>C	NP_612121.1:n.409+55A>C