Canonical Allele Identifier: CA4777583

Gene: NCOA2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.70128911C>T , CM000670.2:g.70128911C>T	GRCh38
NC_000008.10:g.71041146C>T , CM000670.1:g.71041146C>T	GRCh37
NC_000008.9:g.71203700C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452400.7:c.3394G>A MANE Select	ENSP00000399968.2:p.Val1132Ile
ENST00000452400.6:c.3394G>A	ENSP00000399968.2:p.Val1132Ile
ENST00000518287.6:c.*351G>A	ENSP00000430148.2:n.*351G>A
ENST00000518363.2:c.770G>A
NM_006540.2:c.3394G>A	NP_006531.1:p.Val1132Ile
XM_005251128.3:c.3394G>A	XP_005251185.1:p.Val1132Ile
XM_005251129.3:c.3394G>A	XP_005251186.1:p.Val1132Ile
XM_005251130.3:c.3394G>A	XP_005251187.1:p.Val1132Ile
XM_005251131.3:c.3394G>A	XP_005251188.1:p.Val1132Ile
XM_005251133.3:c.3187G>A	XP_005251190.1:p.Val1063Ile
XM_011517436.1:c.3394G>A	XP_011515738.1:p.Val1132Ile
XM_011517437.1:c.3394G>A	XP_011515739.1:p.Val1132Ile
XM_011517438.1:c.3394G>A	XP_011515740.1:p.Val1132Ile
XM_011517439.1:c.3394G>A	XP_011515741.1:p.Val1132Ile
XM_011517440.1:c.2932G>A	XP_011515742.1:p.Val978Ile
NM_001321703.1:c.3394G>A	NP_001308632.1:p.Val1132Ile
NM_001321707.1:c.3394G>A	NP_001308636.1:p.Val1132Ile
NM_001321711.1:c.3187G>A	NP_001308640.1:p.Val1063Ile
NM_001321712.1:c.3187G>A	NP_001308641.1:p.Val1063Ile
NM_001321713.1:c.2932G>A	NP_001308642.1:p.Val978Ile
NM_006540.3:c.3394G>A	NP_006531.1:p.Val1132Ile
XM_017012961.2:c.3394G>A	XP_016868450.1:p.Val1132Ile
XM_017012962.2:c.3394G>A	XP_016868451.1:p.Val1132Ile
XM_017012963.2:c.3394G>A	XP_016868452.1:p.Val1132Ile
XM_017012964.2:c.3394G>A	XP_016868453.1:p.Val1132Ile
XM_017012966.2:c.3394G>A	XP_016868455.1:p.Val1132Ile
XM_017012967.2:c.3394G>A	XP_016868456.1:p.Val1132Ile
XM_017012968.2:c.3394G>A	XP_016868457.1:p.Val1132Ile
XM_017012969.2:c.3394G>A	XP_016868458.1:p.Val1132Ile
XM_017012970.2:c.3394G>A	XP_016868459.1:p.Val1132Ile
XM_017012971.2:c.3394G>A	XP_016868460.1:p.Val1132Ile
XM_017012972.2:c.2932G>A	XP_016868461.1:p.Val978Ile
NM_006540.4:c.3394G>A MANE Select	NP_006531.1:p.Val1132Ile
NM_001321703.2:c.3394G>A	NP_001308632.1:p.Val1132Ile
NM_001321707.2:c.3394G>A	NP_001308636.1:p.Val1132Ile
NM_001321711.2:c.3187G>A	NP_001308640.1:p.Val1063Ile
NM_001321712.2:c.3187G>A	NP_001308641.1:p.Val1063Ile
NM_001321713.2:c.2932G>A	NP_001308642.1:p.Val978Ile