Canonical Allele Identifier: CA431808292

Gene: GIGYF2

Linked Data

• MyVariant Identifiers: chr2:g.233656143C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232791433C>T , CM000664.2:g.232791433C>T	GRCh38
NC_000002.11:g.233656143C>T , CM000664.1:g.233656143C>T	GRCh37
NC_000002.10:g.233364387C>T	NCBI36
NG_011847.1:g.99129C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373563.9:c.1269C>T MANE Select	ENSP00000362664.5:p.Pro423=
ENST00000676848.1:c.615C>T	ENSP00000503313.1:p.Pro205=
ENST00000677450.1:c.750C>T	ENSP00000503420.1:p.Pro250=
ENST00000677591.1:c.525C>T	ENSP00000503061.1:p.Pro175=
ENST00000678230.1:c.762C>T	ENSP00000504272.1:p.Pro254=
ENST00000678339.1:c.525C>T	ENSP00000503437.1:p.Pro175=
ENST00000678466.1:c.525C>T	ENSP00000504219.1:p.Pro175=
ENST00000678885.1:c.525C>T	ENSP00000503563.1:p.Pro175=
ENST00000373563.8:c.1269C>T	ENSP00000362664.4:p.Pro423=
ENST00000409196.7:c.1251C>T	ENSP00000387070.3:p.Pro417=
ENST00000409451.7:c.1332C>T	ENSP00000387170.3:p.Pro444=
ENST00000409480.5:c.1335C>T	ENSP00000386765.1:p.Pro445=
ENST00000409547.5:c.1269C>T	ENSP00000386537.1:p.Pro423=
ENST00000423659.5:c.1098C>T	ENSP00000404195.1:p.Pro366=
ENST00000440945.5:c.1251C>T	ENSP00000410297.1:p.Pro417=
ENST00000458528.1:c.*262C>T	ENSP00000389322.1:n.*262C>T
ENST00000629305.2:c.1335C>T	ENSP00000487548.1:p.Pro445=
NM_001103146.1:c.1269C>T	NP_001096616.1:p.Pro423=
NM_001103147.1:c.1332C>T	NP_001096617.1:p.Pro444=
NM_001103148.1:c.1251C>T	NP_001096618.1:p.Pro417=
NM_015575.3:c.1269C>T	NP_056390.2:p.Pro423=
NR_103492.1:n.1382C>T
NM_001103146.3:c.1269C>T MANE Select	NP_001096616.1:p.Pro423=
NM_001103147.2:c.1332C>T	NP_001096617.1:p.Pro444=
NM_001103148.2:c.1251C>T	NP_001096618.1:p.Pro417=
NM_015575.4:c.1269C>T	NP_056390.2:p.Pro423=