Canonical Allele Identifier: CA1619278987

Gene: MPIG6B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31723930_31723947delinsCAGTGCTTCACGTGCTGG , CM000668.2:g.31723930_31723947delinsCAGTGCTTCACGTGCTGG	GRCh38
NC_000006.11:g.31691707_31691724delinsCAGTGCTTCACGTGCTGG , CM000668.1:g.31691707_31691724delinsCAGTGCTTCACGTGCTGG	GRCh37
NC_000006.10:g.31799686_31799703delinsCAGTGCTTCACGTGCTGG	NCBI36
NG_029044.1:g.5587_5604delinsCAGTGCTTCACGTGCTGG
NG_029044.2:g.5587_5604delinsCAGTGCTTCACGTGCTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649779.1:c.353_370delinsCAGTGCTTCACGTGCTGG MANE Select	ENSP00000497720.1:p.Thr118=
ENST00000375804.6:c.353_370delinsCAGTGCTTCACGTGCTGG	ENSP00000364962.2:p.Thr118=
ENST00000375805.6:c.353_370delinsCAGTGCTTCACGTGCTGG	ENSP00000364963.2:p.Thr118=
ENST00000375806.2:c.353_370delinsCAGTGCTTCACGTGCTGG	ENSP00000364964.2:p.Thr118=
ENST00000375809.7:c.353_370delinsCAGTGCTTCACGTGCTGG	ENSP00000364967.3:p.Thr118=
ENST00000375810.8:c.353_370delinsCAGTGCTTCACGTGCTGG	ENSP00000364968.4:p.Thr118=
ENST00000375814.7:c.353_370delinsCAGTGCTTCACGTGCTGG	ENSP00000364972.3:p.Thr118=
ENST00000460663.5:n.560_577delinsCAGTGCTTCACGTGCTGG
ENST00000466312.5:n.357_374delinsCAGTGCTTCACGTGCTGG
ENST00000471545.1:n.353_370delinsCAGTGCTTCACGTGCTGG
ENST00000480039.5:c.353_370delinsCAGTGCTTCACGTGCTGG	ENSP00000419306.1:p.Thr118=
ENST00000485548.5:c.268+85_268+102delinsCAGTGCTTCACGTGCTGG	ENSP00000420355.1:n.268+85_268+102delinsCAGTGCTTCACGTGCTGG
NM_025260.3:c.353_370delinsCAGTGCTTCACGTGCTGG	NP_079536.2:p.Thr118=
NM_138272.2:c.353_370delinsCAGTGCTTCACGTGCTGG	NP_612116.1:p.Thr118=
NM_138273.2:c.353_370delinsCAGTGCTTCACGTGCTGG	NP_612117.1:p.Thr118=
NM_138274.2:c.353_370delinsCAGTGCTTCACGTGCTGG	NP_612118.1:p.Thr118=
NM_138275.2:c.353_370delinsCAGTGCTTCACGTGCTGG	NP_612119.1:p.Thr118=
NM_138277.2:c.353_370delinsCAGTGCTTCACGTGCTGG	NP_612121.1:p.Thr118=
XM_011514920.1:c.401_418delinsCAGTGCTTCACGTGCTGG	XP_011513222.1:p.Thr134=
XM_011514921.1:c.401_418delinsCAGTGCTTCACGTGCTGG	XP_011513223.1:p.Thr134=
XM_011514920.2:c.401_418delinsCAGTGCTTCACGTGCTGG	XP_011513222.1:p.Thr134=
XM_011514921.2:c.401_418delinsCAGTGCTTCACGTGCTGG	XP_011513223.1:p.Thr134=
XM_017011330.1:c.401_418delinsCAGTGCTTCACGTGCTGG	XP_016866819.1:p.Thr134=
XM_017011331.1:c.353_370delinsCAGTGCTTCACGTGCTGG	XP_016866820.1:p.Thr118=
XM_017011332.1:c.401_418delinsCAGTGCTTCACGTGCTGG	XP_016866821.1:p.Thr134=
XM_017011333.1:c.401_418delinsCAGTGCTTCACGTGCTGG	XP_016866822.1:p.Thr134=
NM_025260.4:c.353_370delinsCAGTGCTTCACGTGCTGG	NP_079536.2:p.Thr118=
NM_138272.3:c.353_370delinsCAGTGCTTCACGTGCTGG MANE Select	NP_612116.1:p.Thr118=
NM_138273.3:c.353_370delinsCAGTGCTTCACGTGCTGG	NP_612117.1:p.Thr118=
NM_138274.3:c.353_370delinsCAGTGCTTCACGTGCTGG	NP_612118.1:p.Thr118=
NM_138275.3:c.353_370delinsCAGTGCTTCACGTGCTGG	NP_612119.1:p.Thr118=
NM_138277.3:c.353_370delinsCAGTGCTTCACGTGCTGG	NP_612121.1:p.Thr118=