Canonical Allele Identifier: CA351018817

Gene: GIGYF2

Linked Data

• MyVariant Identifiers: chr2:g.233674458G>T (hg19) ; chr2:g.232809748G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232809748G>T , CM000664.2:g.232809748G>T	GRCh38
NC_000002.11:g.233674458G>T , CM000664.1:g.233674458G>T	GRCh37
NC_000002.10:g.233382702G>T	NCBI36
NG_011847.1:g.117444G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373563.9:c.1835G>T MANE Select	ENSP00000362664.5:p.Arg612Met
ENST00000676848.1:c.1181G>T	ENSP00000503313.1:p.Arg394Met
ENST00000677450.1:c.1316G>T	ENSP00000503420.1:p.Arg439Met
ENST00000677591.1:c.1091G>T	ENSP00000503061.1:p.Arg364Met
ENST00000678230.1:c.1328G>T	ENSP00000504272.1:p.Arg443Met
ENST00000678339.1:c.1091G>T	ENSP00000503437.1:p.Arg364Met
ENST00000678466.1:c.1091G>T	ENSP00000504219.1:p.Arg364Met
ENST00000678885.1:c.1091G>T	ENSP00000503563.1:p.Arg364Met
ENST00000373563.8:c.1835G>T	ENSP00000362664.4:p.Arg612Met
ENST00000409196.7:c.1817G>T	ENSP00000387070.3:p.Arg606Met
ENST00000409451.7:c.1898G>T	ENSP00000387170.3:p.Arg633Met
ENST00000409480.5:c.1901G>T	ENSP00000386765.1:p.Arg634Met
ENST00000409547.5:c.1835G>T	ENSP00000386537.1:p.Arg612Met
ENST00000423659.5:c.1664G>T	ENSP00000404195.1:p.Arg555Met
ENST00000440945.5:c.1817G>T	ENSP00000410297.1:p.Arg606Met
ENST00000482952.5:n.73G>T
ENST00000629305.2:c.1901G>T	ENSP00000487548.1:p.Arg634Met
NM_001103146.1:c.1835G>T	NP_001096616.1:p.Arg612Met
NM_001103147.1:c.1898G>T	NP_001096617.1:p.Arg633Met
NM_001103148.1:c.1817G>T	NP_001096618.1:p.Arg606Met
NM_015575.3:c.1835G>T	NP_056390.2:p.Arg612Met
NR_103492.1:n.1948G>T
NM_001103146.3:c.1835G>T MANE Select	NP_001096616.1:p.Arg612Met
NM_001103147.2:c.1898G>T	NP_001096617.1:p.Arg633Met
NM_001103148.2:c.1817G>T	NP_001096618.1:p.Arg606Met
NM_015575.4:c.1835G>T	NP_056390.2:p.Arg612Met