Canonical Allele Identifier: CA1019264499

Gene: CHRNA4

Linked Data

• gnomAD v3: 20-63350753-T-TAAGAAA
• gnomAD v4: 20-63350753-T-TAAGAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350753_63350754insAAGAAA , CM000682.2:g.63350753_63350754insAAGAAA	GRCh38
NC_000020.10:g.61982105_61982106insAAGAAA , CM000682.1:g.61982105_61982106insAAGAAA	GRCh37
NC_000020.9:g.61452549_61452550insAAGAAA	NCBI36
NG_011931.1:g.15590_15591insTTTCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.657_658insTTTCTT MANE Select	ENSP00000359285.4:p.Asn219_Thr220insPheLeu
ENST00000370263.8:c.657_658insTTTCTT	ENSP00000359285.4:p.Asn219_Thr220insPheLeu
ENST00000463705.5:n.1305_1306insTTTCTT
ENST00000467563.3:n.727_728insTTTCTT
ENST00000498043.6:c.681_682insTTTCTT
ENST00000615287.4:c.444_445insTTTCTT	ENSP00000483388.1:p.Asn148_Thr149insPheLeu
ENST00000627000.1:c.*346_*347insTTTCTT	ENSP00000486914.1:n.*346_*347insTTTCTT
ENST00000630240.1:n.378_379insTTTCTT
NM_000744.6:c.657_658insTTTCTT	NP_000735.1:p.Asn219_Thr220insPheLeu
NM_001256573.1:c.129_130insTTTCTT	NP_001243502.1:p.Asn43_Thr44insPheLeu
NR_046317.1:n.913_914insTTTCTT
XM_011528524.1:c.444_445insTTTCTT	XP_011526826.1:p.Asn148_Thr149insPheLeu
XM_017027625.2:c.129_130insTTTCTT	XP_016883114.1:p.Asn43_Thr44insPheLeu
XM_024451822.1:c.129_130insTTTCTT	XP_024307590.1:p.Asn43_Thr44insPheLeu
NM_001256573.2:c.129_130insTTTCTT	NP_001243502.1:p.Asn43_Thr44insPheLeu
NR_046317.2:n.866_867insTTTCTT
NM_000744.7:c.657_658insTTTCTT MANE Select	NP_000735.1:p.Asn219_Thr220insPheLeu