Canonical Allele Identifier: CA9330290

Gene: GMIP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.19636711G>A , CM000681.2:g.19636711G>A	GRCh38
NC_000019.9:g.19747520G>A , CM000681.1:g.19747520G>A	GRCh37
NC_000019.8:g.19608520G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_016573.4:c.1323C>T MANE Select	NP_057657.2:p.Ser441=
ENST00000203556.9:c.1323C>T MANE Select	ENSP00000203556.3:p.Ser441=
NM_001288998.1:c.1314C>T	NP_001275927.1:p.Ser438=
NM_001288998.2:c.1314C>T	NP_001275927.1:p.Ser438=
NM_001288999.1:c.1323C>T	NP_001275928.1:p.Ser441=
NM_001288999.2:c.1323C>T	NP_001275928.1:p.Ser441=
NM_016573.3:c.1323C>T	NP_057657.2:p.Ser441=
ENST00000203556.8:c.1323C>T	ENSP00000203556.3:p.Ser441=
ENST00000587238.5:c.1323C>T	ENSP00000467054.1:p.Ser441=
ENST00000587713.1:n.320C>T
ENST00000593186.1:c.554C>T
XM_005259927.1:c.1314C>T	XP_005259984.1:p.Ser438=
XM_005259927.2:c.1314C>T	XP_005259984.1:p.Ser438=
XM_011528048.1:c.960C>T	XP_011526350.1:p.Ser320=
XM_011528048.2:c.960C>T	XP_011526350.1:p.Ser320=
XM_017026861.1:c.1323C>T	XP_016882350.1:p.Ser441=
XM_017026862.1:c.1323C>T	XP_016882351.1:p.Ser441=