Canonical Allele Identifier: CA2656015273
Gene: NEFH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29489604_29489605insCGAGAAGGCCAAGTCCCC , CM000684.2:g.29489604_29489605insCGAGAAGGCCAAGTCCCC GRCh38
NC_000022.10:g.29885593_29885594insCGAGAAGGCCAAGTCCCC , CM000684.1:g.29885593_29885594insCGAGAAGGCCAAGTCCCC GRCh37
NC_000022.9:g.28215593_28215594insCGAGAAGGCCAAGTCCCC NCBI36
NG_008404.1:g.14413_14414insCGAGAAGGCCAAGTCCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000310624.7:c.1964_1965insCGAGAAGGCCAAGTCCCC MANE Select ENSP00000311997.6:p.Pro655_Glu656insGluLysAlaLysSerPro
ENST00000310624.6:c.1964_1965insCGAGAAGGCCAAGTCCCC ENSP00000311997.6:p.Pro655_Glu656insGluLysAlaLysSerPro
NM_021076.3:c.1964_1965insCGAGAAGGCCAAGTCCCC NP_066554.2:p.Pro655_Glu656insGluLysAlaLysSerPro
XM_011530200.1:c.1676_1677insCGAGAAGGCCAAGTCCCC XP_011528502.1:p.Pro559_Glu560insGluLysAlaLysSerPro
XM_011530200.2:c.1676_1677insCGAGAAGGCCAAGTCCCC XP_011528502.1:p.Pro559_Glu560insGluLysAlaLysSerPro
NM_021076.4:c.1964_1965insCGAGAAGGCCAAGTCCCC MANE Select NP_066554.2:p.Pro655_Glu656insGluLysAlaLysSerPro