Canonical Allele Identifier: CA2635576831

Gene: CHRNE

Linked Data

• gnomAD v4: 17-4898402-T-TTAG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4898402_4898403insTAG , CM000679.2:g.4898402_4898403insTAG	GRCh38
NC_000017.10:g.4801697_4801698insTAG , CM000679.1:g.4801697_4801698insTAG	GRCh37
NC_000017.9:g.4742476_4742477insTAG	NCBI36
NG_008029.2:g.9673_9674insCTA
NG_028005.1:g.70063_70064insTAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649488.2:c.*333_*334insCTA MANE Select	ENSP00000497829.1:n.*333_*334insCTA
ENST00000649830.1:c.*451_*452insCTA	ENSP00000496907.1:n.*451_*452insCTA
ENST00000652550.1:n.1541_1542insCTA
ENST00000293780.4:c.*333_*334insCTA	ENSP00000293780.4:n.*333_*334insCTA
ENST00000572438.1:n.1501_1502insCTA
NM_000080.3:c.*333_*334insCTA	NP_000071.1:n.*333_*334insCTA
NM_000080.4:c.*333_*334insCTA MANE Select	NP_000071.1:n.*333_*334insCTA
XM_017024115.1:c.*333_*334insCTA	XP_016879604.1:n.*333_*334insCTA