Canonical Allele Identifier: CA346055696

Gene: NCOA1

Linked Data

• gnomAD v4: 2-24751990-C-T
• COSMIC: COSM1685867 ; COSM1685868
• MyVariant Identifiers: chr2:g.24974859C>T (hg19) ; chr2:g.24751990C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24751990C>T , CM000664.2:g.24751990C>T	GRCh38
NC_000002.11:g.24974859C>T , CM000664.1:g.24974859C>T	GRCh37
NC_000002.10:g.24828363C>T	NCBI36
NG_029014.1:g.172514C>T
NG_029014.2:g.264941C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348332.8:c.3715C>T MANE Select	ENSP00000320940.5:p.Pro1239Ser
ENST00000288599.9:c.3715C>T	ENSP00000288599.5:p.Pro1239Ser
ENST00000348332.7:c.3715C>T	ENSP00000320940.5:p.Pro1239Ser
ENST00000395856.3:c.3715C>T	ENSP00000379197.3:p.Pro1239Ser
ENST00000405141.5:c.3715C>T	ENSP00000385097.1:p.Pro1239Ser
ENST00000406961.5:c.3715C>T	ENSP00000385216.1:p.Pro1239Ser
ENST00000407230.5:c.3262C>T	ENSP00000385195.1:p.Pro1088Ser
NM_003743.4:c.3715C>T	NP_003734.3:p.Pro1239Ser
NM_147223.2:c.3715C>T	NP_671756.1:p.Pro1239Ser
NM_147233.2:c.3715C>T	NP_671766.1:p.Pro1239Ser
XM_005264625.1:c.3715C>T	XP_005264682.1:p.Pro1239Ser
XM_005264626.1:c.3715C>T	XP_005264683.1:p.Pro1239Ser
XM_005264627.1:c.3715C>T	XP_005264684.1:p.Pro1239Ser
XM_005264628.1:c.3715C>T	XP_005264685.1:p.Pro1239Ser
XM_011533141.1:c.3400C>T	XP_011531443.1:p.Pro1134Ser
NM_001362950.1:c.3715C>T	NP_001349879.1:p.Pro1239Ser
NM_001362952.1:c.3715C>T	NP_001349881.1:p.Pro1239Ser
NM_001362954.1:c.3715C>T	NP_001349883.1:p.Pro1239Ser
NM_001362955.1:c.3715C>T	NP_001349884.1:p.Pro1239Ser
NM_003743.5:c.3715C>T MANE Select	NP_003734.3:p.Pro1239Ser
NM_147223.3:c.3715C>T	NP_671756.1:p.Pro1239Ser