Canonical Allele Identifier: CA2733115358
Gene: CHRNE HGNC NCBI

Linked Data

dbSNP Id: rs2151091881

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4898140_4898144dup , CM000679.2:g.4898140_4898144dup GRCh38
NC_000017.10:g.4801435_4801439dup , CM000679.1:g.4801435_4801439dup GRCh37
NC_000017.9:g.4742214_4742218dup NCBI36
NG_008029.2:g.9932_9936dup
NG_028005.1:g.69801_69805dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000649488.2:c.*592_*596dup MANE Select ENSP00000497829.1:n.*592_*596dup
ENST00000649830.1:c.*710_*714dup ENSP00000496907.1:n.*710_*714dup
ENST00000652550.1:n.1800_1804dup
ENST00000293780.4:c.*592_*596dup ENSP00000293780.4:n.*592_*596dup
ENST00000572438.1:n.1760_1764dup
NM_000080.3:c.*592_*596dup NP_000071.1:n.*592_*596dup
NM_000080.4:c.*592_*596dup MANE Select NP_000071.1:n.*592_*596dup
XM_017024115.1:c.*592_*596dup XP_016879604.1:n.*592_*596dup