Canonical Allele Identifier: CA431810023

Gene: GIGYF2

Linked Data

• gnomAD v4: 2-232809773-C-T
• MyVariant Identifiers: chr2:g.233674483C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232809773C>T , CM000664.2:g.232809773C>T	GRCh38
NC_000002.11:g.233674483C>T , CM000664.1:g.233674483C>T	GRCh37
NC_000002.10:g.233382727C>T	NCBI36
NG_011847.1:g.117469C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373563.9:c.1860C>T MANE Select	ENSP00000362664.5:p.Tyr620=
ENST00000676848.1:c.1206C>T	ENSP00000503313.1:p.Tyr402=
ENST00000677450.1:c.1341C>T	ENSP00000503420.1:p.Tyr447=
ENST00000677591.1:c.1116C>T	ENSP00000503061.1:p.Tyr372=
ENST00000678230.1:c.1353C>T	ENSP00000504272.1:p.Tyr451=
ENST00000678339.1:c.1116C>T	ENSP00000503437.1:p.Tyr372=
ENST00000678466.1:c.1116C>T	ENSP00000504219.1:p.Tyr372=
ENST00000678885.1:c.1116C>T	ENSP00000503563.1:p.Tyr372=
ENST00000373563.8:c.1860C>T	ENSP00000362664.4:p.Tyr620=
ENST00000409196.7:c.1842C>T	ENSP00000387070.3:p.Tyr614=
ENST00000409451.7:c.1923C>T	ENSP00000387170.3:p.Tyr641=
ENST00000409480.5:c.1926C>T	ENSP00000386765.1:p.Tyr642=
ENST00000409547.5:c.1860C>T	ENSP00000386537.1:p.Tyr620=
ENST00000423659.5:c.1689C>T	ENSP00000404195.1:p.Tyr563=
ENST00000440945.5:c.1842C>T	ENSP00000410297.1:p.Tyr614=
ENST00000482952.5:n.98C>T
ENST00000629305.2:c.1926C>T	ENSP00000487548.1:p.Tyr642=
NM_001103146.1:c.1860C>T	NP_001096616.1:p.Tyr620=
NM_001103147.1:c.1923C>T	NP_001096617.1:p.Tyr641=
NM_001103148.1:c.1842C>T	NP_001096618.1:p.Tyr614=
NM_015575.3:c.1860C>T	NP_056390.2:p.Tyr620=
NR_103492.1:n.1973C>T
NM_001103146.3:c.1860C>T MANE Select	NP_001096616.1:p.Tyr620=
NM_001103147.2:c.1923C>T	NP_001096617.1:p.Tyr641=
NM_001103148.2:c.1842C>T	NP_001096618.1:p.Tyr614=
NM_015575.4:c.1860C>T	NP_056390.2:p.Tyr620=