Canonical Allele Identifier: CA1750623624
Gene: CNTNAP2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.147132181_147132182delinsTG , CM000669.2:g.147132181_147132182delinsTG GRCh38
NC_000007.13:g.146829273_146829274delinsTG , CM000669.1:g.146829273_146829274delinsTG GRCh37
NC_000007.12:g.146460206_146460207delinsTG NCBI36
NG_007092.2:g.1020821_1020822delinsTG
NG_007092.3:g.1021181_1021182delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000361727.8:c.1084-64_1084-63delinsTG MANE Select ENSP00000354778.3:n.1084-64_1084-63delinsTG
ENST00000636561.1:n.987-64_987-63delinsTG
ENST00000636870.1:n.946-64_946-63delinsTG
ENST00000637150.1:n.1013-64_1013-63delinsTG
ENST00000637694.1:n.987-64_987-63delinsTG
ENST00000637825.1:n.567-64_567-63delinsTG
ENST00000638117.1:n.987-64_987-63delinsTG
ENST00000361727.7:c.1084-64_1084-63delinsTG ENSP00000354778.3:n.1084-64_1084-63delinsTG
NM_014141.5:c.1084-64_1084-63delinsTG NP_054860.1:n.1084-64_1084-63delinsTG
XM_017011950.2:c.1084-64_1084-63delinsTG XP_016867439.1:n.1084-64_1084-63delinsTG
NM_014141.6:c.1084-64_1084-63delinsTG MANE Select NP_054860.1:n.1084-64_1084-63delinsTG
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