Canonical Allele Identifier: CA6046741

Gene: AHNAK

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62533220G>C , CM000673.2:g.62533220G>C	GRCh38
NC_000011.9:g.62300692G>C , CM000673.1:g.62300692G>C	GRCh37
NC_000011.8:g.62057268G>C	NCBI36
NG_051822.1:g.18641C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001620.3:c.1197C>G MANE Select	NP_001611.1:p.Ala399=
ENST00000378024.9:c.1197C>G MANE Select	ENSP00000367263.4:p.Ala399=
NM_001346445.1:c.1197C>G	NP_001333374.1:p.Ala399=
NM_001346445.2:c.1197C>G	NP_001333374.1:p.Ala399=
NM_001346446.1:c.1197C>G	NP_001333375.1:p.Ala399=
NM_001346446.2:c.1197C>G	NP_001333375.1:p.Ala399=
NM_001620.2:c.1197C>G	NP_001611.1:p.Ala399=
NM_024060.3:c.342+1783C>G	NP_076965.2:n.342+1783C>G
NM_024060.4:c.342+1783C>G	NP_076965.2:n.342+1783C>G
ENST00000257247.11:c.342+1783C>G	ENSP00000257247.7:n.342+1783C>G
ENST00000378024.8:c.1197C>G	ENSP00000367263.4:p.Ala399=
ENST00000530124.5:c.342+1783C>G	ENSP00000433789.1:n.342+1783C>G
ENST00000533365.5:c.342+1783C>G	ENSP00000433635.1:n.342+1783C>G
XM_005274240.1:c.1197C>G	XP_005274297.1:p.Ala399=
XM_005274241.1:c.1197C>G	XP_005274298.1:p.Ala399=
XM_005274242.1:c.1197C>G	XP_005274299.1:p.Ala399=
XM_005274243.1:c.1197C>G	XP_005274300.1:p.Ala399=
XM_005274244.1:c.1197C>G	XP_005274301.1:p.Ala399=
XM_005274245.1:c.1197C>G	XP_005274302.1:p.Ala399=
XM_011545249.1:c.1197C>G	XP_011543551.1:p.Ala399=
XM_011545250.1:c.1197C>G	XP_011543552.1:p.Ala399=
XM_017018270.1:c.1197C>G	XP_016873759.1:p.Ala399=