Canonical Allele Identifier: CA2685448889
Gene: CNTNAP2 HGNC NCBI

Linked Data

gnomAD v4: 7-147132235-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.147132235T>A , CM000669.2:g.147132235T>A GRCh38
NC_000007.13:g.146829327T>A , CM000669.1:g.146829327T>A GRCh37
NC_000007.12:g.146460260T>A NCBI36
NG_007092.2:g.1020875T>A
NG_007092.3:g.1021235T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000361727.8:c.1084-10T>A MANE Select ENSP00000354778.3:n.1084-10T>A
ENST00000636561.1:n.987-10T>A
ENST00000636870.1:n.946-10T>A
ENST00000637150.1:n.1013-10T>A
ENST00000637694.1:n.987-10T>A
ENST00000637825.1:n.567-10T>A
ENST00000638117.1:n.987-10T>A
ENST00000361727.7:c.1084-10T>A ENSP00000354778.3:n.1084-10T>A
NM_014141.5:c.1084-10T>A NP_054860.1:n.1084-10T>A
XM_017011950.2:c.1084-10T>A XP_016867439.1:n.1084-10T>A
NM_014141.6:c.1084-10T>A MANE Select NP_054860.1:n.1084-10T>A
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