Canonical Allele Identifier: CA3533745

Gene: CYFIP2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157326276T>C , CM000667.2:g.157326276T>C	GRCh38
NC_000005.9:g.156753284T>C , CM000667.1:g.156753284T>C	GRCh37
NC_000005.8:g.156685862T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698888.1:c.2154+9T>C	ENSP00000514007.1:n.2154+9T>C
ENST00000620254.5:c.2079+9T>C MANE Select	ENSP00000479968.1:n.2079+9T>C
ENST00000435847.6:c.1671+9T>C	ENSP00000403793.3:n.1671+9T>C
ENST00000518555.1:n.668+9T>C
ENST00000520960.2:c.538+9T>C	ENSP00000482739.1:n.538+9T>C
ENST00000521420.5:c.2001+9T>C	ENSP00000430904.1:n.2001+9T>C
ENST00000522463.5:c.1491+9T>C	ENSP00000428009.1:n.1491+9T>C
ENST00000616178.4:c.2154+9T>C	ENSP00000479719.1:n.2154+9T>C
ENST00000618329.4:c.2079+9T>C	ENSP00000484819.1:n.2079+9T>C
ENST00000620254.4:c.2079+9T>C	ENSP00000479968.1:n.2079+9T>C
ENST00000620969.4:c.-67+9T>C	ENSP00000483307.1:n.-67+9T>C
NM_001037333.2:c.2079+9T>C	NP_001032410.1:n.2079+9T>C
NM_001291721.1:c.2001+9T>C	NP_001278650.1:n.2001+9T>C
NM_001291722.1:c.2154+9T>C	NP_001278651.1:n.2154+9T>C
NM_014376.3:c.2079+9T>C	NP_055191.2:n.2079+9T>C
XM_011534516.1:c.2079+9T>C	XP_011532818.1:n.2079+9T>C
XM_011534517.1:c.1866+9T>C	XP_011532819.1:n.1866+9T>C
XM_011534516.3:c.2079+9T>C	XP_011532818.1:n.2079+9T>C
XM_017009341.1:c.2079+9T>C	XP_016864830.1:n.2079+9T>C
XM_017009342.1:c.1866+9T>C	XP_016864831.1:n.1866+9T>C
XR_001742052.2:n.2184+9T>C
NM_001037333.3:c.2079+9T>C MANE Select	NP_001032410.1:n.2079+9T>C
NM_001291721.2:c.2001+9T>C	NP_001278650.1:n.2001+9T>C
NM_001291722.2:c.2154+9T>C	NP_001278651.1:n.2154+9T>C
NM_014376.4:c.2079+9T>C	NP_055191.2:n.2079+9T>C