Canonical Allele Identifier: CA60857605
Community Standard Title: NM_000079.4(CHRNA1):c.44-302_44-297dup
Gene: CHRNA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.174759954_174759959dup , CM000664.2:g.174759954_174759959dup GRCh38
NC_000002.11:g.175624682_175624687dup , CM000664.1:g.175624682_175624687dup GRCh37
NC_000002.10:g.175332928_175332933dup NCBI36
NG_008172.1:g.9538_9543dup

Transcript Alleles

HGVS Amino-acid Change
NM_000079.4:c.44-302_44-297dup MANE Select NP_000070.1:n.44-302_44-297dup
ENST00000348749.9:c.44-302_44-297dup MANE Select ENSP00000261008.5:n.44-302_44-297dup
NM_000079.3:c.44-302_44-297dup NP_000070.1:n.44-302_44-297dup
NM_001039523.2:c.44-302_44-297dup NP_001034612.1:n.44-302_44-297dup
NM_001039523.3:c.44-302_44-297dup NP_001034612.1:n.44-302_44-297dup
ENST00000261007.9:c.44-302_44-297dup ENSP00000261007.5:n.44-302_44-297dup
ENST00000409219.5:c.44-302_44-297dup ENSP00000386611.1:n.44-302_44-297dup
ENST00000409323.1:c.44-302_44-297dup ENSP00000386684.1:n.44-302_44-297dup
ENST00000409542.5:c.44-302_44-297dup ENSP00000387026.1:n.44-302_44-297dup
ENST00000435083.5:c.44-302_44-297dup ENSP00000395805.1:n.44-302_44-297dup
ENST00000636168.2:c.-446-302_-446-297dup ENSP00000490338.2:n.-446-302_-446-297dup
ENST00000672640.1:c.-446-302_-446-297dup ENSP00000500507.1:n.-446-302_-446-297dup