Canonical Allele Identifier: CA396823039
Gene: CNTNAP4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.76558645A>G , CM000678.2:g.76558645A>G GRCh38
NC_000016.9:g.76592542A>G , CM000678.1:g.76592542A>G GRCh37
NC_000016.8:g.75150043A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_033401.5:c.3889A>G MANE Select NP_207837.2:p.Asn1297Asp
ENST00000611870.5:c.3889A>G MANE Select ENSP00000479811.1:p.Asn1297Asp
NM_001322178.1:c.3739A>G NP_001309107.1:p.Asn1247Asp
NM_001322178.2:c.3739A>G NP_001309107.1:p.Asn1247Asp
NM_001322179.1:c.3649A>G NP_001309108.1:p.Asn1217Asp
NM_001322179.2:c.3649A>G NP_001309108.1:p.Asn1217Asp
NM_001322180.1:c.3502A>G NP_001309109.1:p.Asn1168Asp
NM_001322180.2:c.3502A>G NP_001309109.1:p.Asn1168Asp
NM_001322181.1:c.3886A>G NP_001309110.1:p.Asn1296Asp
NM_001322181.2:c.3886A>G NP_001309110.1:p.Asn1296Asp
NM_001322187.1:c.2473A>G NP_001309116.1:p.Asn825Asp
NM_001322187.2:c.2473A>G NP_001309116.1:p.Asn825Asp
NM_001322188.1:c.3784A>G NP_001309117.1:p.Asn1262Asp
NM_001322188.2:c.3784A>G NP_001309117.1:p.Asn1262Asp
NM_001322189.1:c.3625A>G NP_001309118.1:p.Asn1209Asp
NM_001322189.2:c.3625A>G NP_001309118.1:p.Asn1209Asp
NM_001322190.1:c.3745A>G NP_001309119.1:p.Asn1249Asp
NM_001322190.2:c.3745A>G NP_001309119.1:p.Asn1249Asp
NM_001322191.1:c.2962A>G NP_001309120.1:p.Asn988Asp
NM_001322191.2:c.2962A>G NP_001309120.1:p.Asn988Asp
NM_033401.3:c.3889A>G NP_207837.2:p.Asn1297Asp
NM_033401.4:c.3889A>G NP_207837.2:p.Asn1297Asp
NM_138994.3:c.3670A>G NP_620481.2:p.Asn1224Asp
NM_138994.4:c.3670A>G NP_620481.2:p.Asn1224Asp
NM_138994.5:c.3670A>G NP_620481.2:p.Asn1224Asp
NR_136210.1:n.4477A>G
NR_136210.2:n.4293A>G
NR_136213.1:n.4376A>G
NR_136213.2:n.4192A>G
NR_136216.1:n.4564A>G
NR_136216.2:n.4380A>G
ENST00000307431.12:c.3889A>G ENSP00000306893.9:p.Asn1297Asp
ENST00000377504.8:c.3745A>G ENSP00000439733.2:p.Asn1249Asp
ENST00000476707.1:c.3898A>G ENSP00000417628.1:p.Asn1300Asp
ENST00000478060.5:c.3670A>G ENSP00000418741.1:p.Asn1224Asp
ENST00000563764.2:c.157+4738A>G ENSP00000455258.1:n.157+4738A>G
ENST00000611870.4:c.3889A>G ENSP00000479811.1:p.Asn1297Asp
ENST00000619533.1:n.1270A>G
ENST00000622250.4:c.3745A>G ENSP00000477698.1:p.Asn1249Asp
ENST00000655556.1:c.3733+4738A>G ENSP00000499374.1:n.3733+4738A>G
XM_011523402.1:c.3898A>G XP_011521704.1:p.Asn1300Asp
XM_011523403.1:c.3814A>G XP_011521705.1:p.Asn1272Asp
XM_011523403.2:c.3814A>G XP_011521705.1:p.Asn1272Asp
XM_011523404.1:c.2962A>G XP_011521706.1:p.Asn988Asp
XM_017023805.2:c.2962A>G XP_016879294.1:p.Asn988Asp
XR_001752013.1:n.4222A>G