Canonical Allele Identifier: CA1532357

Gene: GREB1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.11618857C>T , CM000664.2:g.11618857C>T	GRCh38
NC_000002.11:g.11758983C>T , CM000664.1:g.11758983C>T	GRCh37
NC_000002.10:g.11676434C>T	NCBI36
NG_029429.1:g.89742C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_014668.4:c.3982C>T MANE Select	NP_055483.2:p.Arg1328Trp
ENST00000381486.7:c.3982C>T MANE Select	ENSP00000370896.2:p.Arg1328Trp
NM_014668.3:c.3982C>T	NP_055483.2:p.Arg1328Trp
ENST00000234142.9:c.3982C>T	ENSP00000234142.5:p.Arg1328Trp
ENST00000381486.6:c.3982C>T	ENSP00000370896.2:p.Arg1328Trp
ENST00000396123.2:c.976C>T	ENSP00000379429.1:p.Arg326Trp
XM_005246192.3:c.3982C>T	XP_005246249.1:p.Arg1328Trp
XM_005246192.4:c.3982C>T	XP_005246249.1:p.Arg1328Trp
XM_005246196.2:c.1249C>T	XP_005246253.1:p.Arg417Trp
XM_005246196.3:c.1249C>T	XP_005246253.1:p.Arg417Trp
XM_005246197.1:c.976C>T	XP_005246254.1:p.Arg326Trp
XM_011510418.1:c.3979C>T	XP_011508720.1:p.Arg1327Trp
XM_011510418.3:c.3979C>T	XP_011508720.1:p.Arg1327Trp
XM_011510419.1:c.3979C>T	XP_011508721.1:p.Arg1327Trp
XM_011510419.3:c.3979C>T	XP_011508721.1:p.Arg1327Trp
XM_011510420.1:c.3952C>T	XP_011508722.1:p.Arg1318Trp
XM_011510421.1:c.3982C>T	XP_011508723.1:p.Arg1328Trp
XM_011510422.1:c.1354C>T	XP_011508724.1:p.Arg452Trp
XM_011510422.2:c.1354C>T	XP_011508724.1:p.Arg452Trp
XM_024453250.1:c.3982C>T	XP_024309018.1:p.Arg1328Trp
XM_024453251.1:c.3982C>T	XP_024309019.1:p.Arg1328Trp
XM_024453252.1:c.3982C>T	XP_024309020.1:p.Arg1328Trp
XM_024453253.1:c.3982C>T	XP_024309021.1:p.Arg1328Trp
XM_024453254.1:c.3982C>T	XP_024309022.1:p.Arg1328Trp
XM_024453255.1:c.3982C>T	XP_024309023.1:p.Arg1328Trp
XM_024453256.1:c.3982C>T	XP_024309024.1:p.Arg1328Trp
XR_001739081.2:n.4912C>T