Canonical Allele Identifier: CA2678022681

Gene: MPIG6B

Linked Data

• gnomAD v4: 6-31724015-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31724015A>T , CM000668.2:g.31724015A>T	GRCh38
NC_000006.11:g.31691792A>T , CM000668.1:g.31691792A>T	GRCh37
NC_000006.10:g.31799771A>T	NCBI36
NG_029044.1:g.5672A>T
NG_029044.2:g.5672A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649779.1:c.409+29A>T MANE Select	ENSP00000497720.1:n.409+29A>T
ENST00000375804.6:c.409+29A>T	ENSP00000364962.2:n.409+29A>T
ENST00000375805.6:c.409+29A>T	ENSP00000364963.2:n.409+29A>T
ENST00000375806.2:c.409+29A>T	ENSP00000364964.2:n.409+29A>T
ENST00000375809.7:c.409+29A>T	ENSP00000364967.3:n.409+29A>T
ENST00000375810.8:c.409+29A>T	ENSP00000364968.4:n.409+29A>T
ENST00000375814.7:c.409+29A>T	ENSP00000364972.3:n.409+29A>T
ENST00000460663.5:n.616+29A>T
ENST00000466312.5:n.413+29A>T
ENST00000471545.1:n.409+29A>T
ENST00000480039.5:c.409+29A>T	ENSP00000419306.1:n.409+29A>T
ENST00000485548.5:c.269-144A>T	ENSP00000420355.1:n.269-144A>T
NM_025260.3:c.409+29A>T	NP_079536.2:n.409+29A>T
NM_138272.2:c.409+29A>T	NP_612116.1:n.409+29A>T
NM_138273.2:c.409+29A>T	NP_612117.1:n.409+29A>T
NM_138274.2:c.409+29A>T	NP_612118.1:n.409+29A>T
NM_138275.2:c.409+29A>T	NP_612119.1:n.409+29A>T
NM_138277.2:c.409+29A>T	NP_612121.1:n.409+29A>T
XM_011514920.1:c.457+29A>T	XP_011513222.1:n.457+29A>T
XM_011514921.1:c.457+29A>T	XP_011513223.1:n.457+29A>T
XM_011514920.2:c.457+29A>T	XP_011513222.1:n.457+29A>T
XM_011514921.2:c.457+29A>T	XP_011513223.1:n.457+29A>T
XM_017011330.1:c.457+29A>T	XP_016866819.1:n.457+29A>T
XM_017011331.1:c.409+29A>T	XP_016866820.1:n.409+29A>T
XM_017011332.1:c.457+29A>T	XP_016866821.1:n.457+29A>T
XM_017011333.1:c.457+29A>T	XP_016866822.1:n.457+29A>T
NM_025260.4:c.409+29A>T	NP_079536.2:n.409+29A>T
NM_138272.3:c.409+29A>T MANE Select	NP_612116.1:n.409+29A>T
NM_138273.3:c.409+29A>T	NP_612117.1:n.409+29A>T
NM_138274.3:c.409+29A>T	NP_612118.1:n.409+29A>T
NM_138275.3:c.409+29A>T	NP_612119.1:n.409+29A>T
NM_138277.3:c.409+29A>T	NP_612121.1:n.409+29A>T