Canonical Allele Identifier: CA1540561678

Gene: FYB1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.39119621C= , CM000667.2:g.39119621C=	GRCh38
NC_000005.9:g.39119723C= , CM000667.1:g.39119723C=	GRCh37
NC_000005.8:g.39155480C=	NCBI36
NG_029596.1:g.156037G=
NG_029596.2:g.156037G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351578.12:c.2014G=	ENSP00000316460.7:p.Val672=
ENST00000512982.4:c.2152G= MANE Select	ENSP00000425845.3:p.Val718=
ENST00000646045.2:c.2182G=	ENSP00000493623.1:p.Val728=
ENST00000646444.1:c.338G=
ENST00000647313.1:n.146G=
ENST00000351578.10:c.2014G=	ENSP00000316460.7:p.Val672=
ENST00000505428.5:c.2152G=	ENSP00000427114.1:p.Val718=
ENST00000512982.2:c.2182G=	ENSP00000425845.2:p.Val728=
ENST00000515010.5:c.2014G=	ENSP00000426346.1:p.Val672=
NM_001243093.1:c.2182G=	NP_001230022.1:p.Val728=
NM_001465.4:c.2152G=	NP_001456.3:p.Val718=
NM_199335.3:c.2014G=	NP_955367.1:p.Val672=
XM_006714464.2:c.2152G=	XP_006714527.1:p.Val718=
XM_006714465.2:c.2152G=	XP_006714528.1:p.Val718=
XM_006714466.2:c.2152G=	XP_006714529.1:p.Val718=
XM_011514008.1:c.2182G=	XP_011512310.1:p.Val728=
XM_011514009.1:c.2152G=	XP_011512311.1:p.Val718=
XM_011514010.1:c.2152G=	XP_011512312.1:p.Val718=
XM_011514011.1:c.2044G=	XP_011512313.1:p.Val682=
NM_001349333.1:c.2152G=	NP_001336262.1:p.Val718=
NM_001465.5:c.2152G=	NP_001456.3:p.Val718=
NM_018594.2:c.2044G=	NP_061064.2:p.Val682=
NM_199335.4:c.2014G=	NP_955367.1:p.Val672=
XM_006714464.3:c.2152G=	XP_006714527.1:p.Val718=
XM_011514008.3:c.2182G=	XP_011512310.1:p.Val728=
XM_011514011.2:c.2044G=	XP_011512313.1:p.Val682=
NM_001243093.2:c.2182G=	NP_001230022.1:p.Val728=
NM_001349333.2:c.2152G=	NP_001336262.1:p.Val718=
NM_001465.6:c.2152G= MANE Select	NP_001456.3:p.Val718=
NM_199335.5:c.2014G=	NP_955367.1:p.Val672=