Canonical Allele Identifier: CA1239046818

Gene: NCOA1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24768609_24768612delinsGAAA , CM000664.2:g.24768609_24768612delinsGAAA	GRCh38
NC_000002.11:g.24991478_24991481delinsGAAA , CM000664.1:g.24991478_24991481delinsGAAA	GRCh37
NC_000002.10:g.24844982_24844985delinsGAAA	NCBI36
NG_029014.1:g.189133_189136delinsGAAA
NG_029014.2:g.281560_281563delinsGAAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000348332.8:c.*218_*221delinsGAAA MANE Select	ENSP00000320940.5:n.*218_*221delinsGAAA
ENST00000288599.9:c.*401_*404delinsGAAA	ENSP00000288599.5:n.*401_*404delinsGAAA
ENST00000348332.7:c.*218_*221delinsGAAA	ENSP00000320940.5:n.*218_*221delinsGAAA
ENST00000395856.3:c.*218_*221delinsGAAA	ENSP00000379197.3:n.*218_*221delinsGAAA
ENST00000405141.5:c.*401_*404delinsGAAA	ENSP00000385097.1:n.*401_*404delinsGAAA
ENST00000406961.5:c.*218_*221delinsGAAA	ENSP00000385216.1:n.*218_*221delinsGAAA
NM_003743.4:c.*218_*221delinsGAAA	NP_003734.3:n.*218_*221delinsGAAA
NM_147223.2:c.*401_*404delinsGAAA	NP_671756.1:n.*401_*404delinsGAAA
NM_147233.2:c.*218_*221delinsGAAA	NP_671766.1:n.*218_*221delinsGAAA
XM_005264625.1:c.*218_*221delinsGAAA	XP_005264682.1:n.*218_*221delinsGAAA
XM_005264626.1:c.*218_*221delinsGAAA	XP_005264683.1:n.*218_*221delinsGAAA
XM_005264627.1:c.*401_*404delinsGAAA	XP_005264684.1:n.*401_*404delinsGAAA
XM_005264628.1:c.*398_*401delinsGAAA	XP_005264685.1:n.*398_*401delinsGAAA
XM_011533141.1:c.*218_*221delinsGAAA	XP_011531443.1:n.*218_*221delinsGAAA
NM_001362950.1:c.*401_*404delinsGAAA	NP_001349879.1:n.*401_*404delinsGAAA
NM_001362952.1:c.*401_*404delinsGAAA	NP_001349881.1:n.*401_*404delinsGAAA
NM_001362954.1:c.*398_*401delinsGAAA	NP_001349883.1:n.*398_*401delinsGAAA
NM_001362955.1:c.*401_*404delinsGAAA	NP_001349884.1:n.*401_*404delinsGAAA
NM_003743.5:c.*218_*221delinsGAAA MANE Select	NP_003734.3:n.*218_*221delinsGAAA
NM_147223.3:c.*401_*404delinsGAAA	NP_671756.1:n.*401_*404delinsGAAA