Canonical Allele Identifier: CA1364760147

Gene: TWF2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52230891T= , CM000665.2:g.52230891T=	GRCh38
NC_000003.11:g.52264907T= , CM000665.1:g.52264907T=	GRCh37
NC_000003.10:g.52239947T=	NCBI36
NG_033933.1:g.273A=

Transcript Alleles

HGVS	Amino-acid Change
NM_007284.4:c.588A= MANE Select	NP_009215.1:p.Lys196=
ENST00000305533.10:c.588A= MANE Select	ENSP00000303908.4:p.Lys196=
NM_007284.3:c.588A=	NP_009215.1:p.Lys196=
ENST00000305533.9:c.588A=	ENSP00000303908.4:p.Lys196=
ENST00000472755.2:n.721A=
ENST00000494383.1:c.169A=
ENST00000499914.2:c.588A=	ENSP00000426464.1:p.Lys196=
ENST00000676552.1:n.1278A=
ENST00000676800.1:n.718A=
ENST00000676988.1:c.588A=	ENSP00000503120.1:p.Lys196=
ENST00000676989.1:c.*427A=	ENSP00000503679.1:n.*427A=
ENST00000677058.1:n.849A=
ENST00000677127.1:n.713A=
ENST00000678330.1:c.588A=	ENSP00000504436.1:p.Lys196=
ENST00000678352.1:n.647A=
ENST00000678549.1:c.*427A=	ENSP00000504044.1:n.*427A=
ENST00000678681.1:n.829A=
ENST00000678700.1:n.721A=
ENST00000678838.1:c.294A=	ENSP00000504408.1:p.Lys98=
ENST00000678882.1:n.640A=
ENST00000679180.1:n.636A=
ENST00000679296.1:c.294A=	ENSP00000504576.1:p.Lys98=