Canonical Allele Identifier: CA425170816

Gene: NCOA1

Linked Data

• MyVariant Identifiers: chr2:g.24974858T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24751989T>G , CM000664.2:g.24751989T>G	GRCh38
NC_000002.11:g.24974858T>G , CM000664.1:g.24974858T>G	GRCh37
NC_000002.10:g.24828362T>G	NCBI36
NG_029014.1:g.172513T>G
NG_029014.2:g.264940T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000348332.8:c.3714T>G MANE Select	ENSP00000320940.5:p.Val1238=
ENST00000288599.9:c.3714T>G	ENSP00000288599.5:p.Val1238=
ENST00000348332.7:c.3714T>G	ENSP00000320940.5:p.Val1238=
ENST00000395856.3:c.3714T>G	ENSP00000379197.3:p.Val1238=
ENST00000405141.5:c.3714T>G	ENSP00000385097.1:p.Val1238=
ENST00000406961.5:c.3714T>G	ENSP00000385216.1:p.Val1238=
ENST00000407230.5:c.3261T>G	ENSP00000385195.1:p.Val1087=
NM_003743.4:c.3714T>G	NP_003734.3:p.Val1238=
NM_147223.2:c.3714T>G	NP_671756.1:p.Val1238=
NM_147233.2:c.3714T>G	NP_671766.1:p.Val1238=
XM_005264625.1:c.3714T>G	XP_005264682.1:p.Val1238=
XM_005264626.1:c.3714T>G	XP_005264683.1:p.Val1238=
XM_005264627.1:c.3714T>G	XP_005264684.1:p.Val1238=
XM_005264628.1:c.3714T>G	XP_005264685.1:p.Val1238=
XM_011533141.1:c.3399T>G	XP_011531443.1:p.Val1133=
NM_001362950.1:c.3714T>G	NP_001349879.1:p.Val1238=
NM_001362952.1:c.3714T>G	NP_001349881.1:p.Val1238=
NM_001362954.1:c.3714T>G	NP_001349883.1:p.Val1238=
NM_001362955.1:c.3714T>G	NP_001349884.1:p.Val1238=
NM_003743.5:c.3714T>G MANE Select	NP_003734.3:p.Val1238=
NM_147223.3:c.3714T>G	NP_671756.1:p.Val1238=