Canonical Allele Identifier: CA2637974409
Gene: CNTNAP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42687749_42687778dup , CM000679.2:g.42687749_42687778dup GRCh38
NC_000017.10:g.40839767_40839796dup , CM000679.1:g.40839767_40839796dup GRCh37
NC_000017.9:g.38093293_38093322dup NCBI36
NG_042091.1:g.10136_10165dup

Transcript Alleles

HGVS Amino-acid change
ENST00000264638.9:c.1074_1103dup MANE Select ENSP00000264638.3:p.Pro368_His369insValPr...
ENST00000264638.8:c.1074_1103dup ENSP00000264638.3:p.Pro368_His369insValPr...
ENST00000586801.1:n.489_518dup
ENST00000591662.1:c.1074_1103dup ENSP00000466571.1:p.Pro368_His369insValPr...
NM_003632.2:c.1074_1103dup NP_003623.1:p.Pro368_His369insValProHisPr...
XM_005257748.3:c.846_875dup XP_005257805.1:p.Pro292_His293insValProHi...
XM_005257748.4:c.846_875dup XP_005257805.1:p.Pro292_His293insValProHi...
XM_017025238.1:c.1074_1103dup XP_016880727.1:p.Pro368_His369insValProHi...
XM_024451011.1:c.1074_1103dup XP_024306779.1:p.Pro368_His369insValProHi...
NM_003632.3:c.1074_1103dup MANE Select NP_003623.1:p.Pro368_His369insValProHisPr...