Canonical Allele Identifier: CA2338450309

Gene: FOSB ERCC1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45475117A= , CM000681.2:g.45475117A=	GRCh38
NC_000019.9:g.45978375A= , CM000681.1:g.45978375A=	GRCh37
NC_000019.8:g.50670215A=	NCBI36
NG_015839.2:g.8712T=
NG_029675.1:g.12123A=

Transcript Alleles

HGVS	Amino-acid Change
NM_006732.3:c.*2105A= (FOSB) MANE Select	NP_006723.2:n.*2105A=
ENST00000353609.8:c.*2105A= (FOSB) MANE Select	ENSP00000245919.3:n.*2105A=
NM_001114171.1:c.*2105A= (FOSB)	NP_001107643.1:n.*2105A=
NM_001114171.2:c.*2105A= (FOSB)	NP_001107643.1:n.*2105A=
NM_006732.2:c.*2105A= (FOSB)	NP_006723.2:n.*2105A=
ENST00000353609.7:c.*2105A= (FOSB)	ENSP00000245919.3:n.*2105A=
ENST00000417353.6:c.*2105A= (FOSB)	ENSP00000407207.1:n.*2105A=
ENST00000423698.6:c.-8+3619T= (ERCC1)	ENSP00000394875.2:n.-8+3619T=
ENST00000443841.6:c.*2105A= (FOSB)	ENSP00000414177.1:n.*2105A=
ENST00000585836.5:c.*2105A= (FOSB)	ENSP00000467497.1:n.*2105A=
ENST00000586615.5:c.*2105A= (FOSB)	ENSP00000468207.1:n.*2105A=
ENST00000591858.5:c.*2105A= (FOSB)	ENSP00000466530.1:n.*2105A=
XM_005258636.3:c.-8+3619T= (ERCC1)	XP_005258693.1:n.-8+3619T=
XM_005258636.4:c.-8+3619T= (ERCC1)	XP_005258693.1:n.-8+3619T=
XM_005258691.1:c.*2268A= (FOSB)	XP_005258748.1:n.*2268A=
XM_017026464.1:c.-8+3619T= (ERCC1)	XP_016881953.1:n.-8+3619T=