Canonical Allele Identifier: CA2587988770

Gene: FCER2

Linked Data

• gnomAD v4: 19-7690081-G-GGT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7690081_7690082insGT , CM000681.2:g.7690081_7690082insGT	GRCh38
NC_000019.9:g.7754967_7754968insGT , CM000681.1:g.7754967_7754968insGT	GRCh37
NC_000019.8:g.7660967_7660968insGT	NCBI36
NG_029554.1:g.17065_17066insAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597921.6:c.728+77_728+78insAC MANE Select	ENSP00000471974.1:n.728+77_728+78insAC
ENST00000346664.9:c.728+77_728+78insAC	ENSP00000264072.6:n.728+77_728+78insAC
ENST00000360067.8:c.725+77_725+78insAC	ENSP00000353178.4:n.725+77_725+78insAC
ENST00000597312.5:n.1253+77_1253+78insAC
ENST00000597921.5:c.728+77_728+78insAC	ENSP00000471974.1:n.728+77_728+78insAC
ENST00000597934.1:n.1090+77_1090+78insAC
ENST00000598803.5:n.1223+77_1223+78insAC
NM_001207019.2:c.725+77_725+78insAC	NP_001193948.2:n.725+77_725+78insAC
NM_001220500.1:c.728+77_728+78insAC	NP_001207429.1:n.728+77_728+78insAC
NM_002002.4:c.728+77_728+78insAC	NP_001993.2:n.728+77_728+78insAC
XM_005272462.3:c.728+77_728+78insAC	XP_005272519.1:n.728+77_728+78insAC
XM_005272462.4:c.728+77_728+78insAC	XP_005272519.1:n.728+77_728+78insAC
NM_001220500.2:c.728+77_728+78insAC MANE Select	NP_001207429.1:n.728+77_728+78insAC
NM_001207019.3:c.725+77_725+78insAC	NP_001193948.2:n.725+77_725+78insAC
NM_002002.5:c.728+77_728+78insAC	NP_001993.2:n.728+77_728+78insAC