Canonical Allele Identifier: CA1926883405

Gene: PANK1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89612776G= , CM000672.2:g.89612776G=	GRCh38
NC_000010.10:g.91372533G= , CM000672.1:g.91372533G=	GRCh37
NC_000010.9:g.91362513G=	NCBI36
NG_029474.1:g.37797C=

Transcript Alleles

HGVS	Amino-acid Change
NM_148977.3:c.293-728C= MANE Select	NP_683878.2:n.293-728C=
ENST00000307534.10:c.293-728C= MANE Select	ENSP00000302108.5:n.293-728C=
NM_138316.3:c.29-728C=	NP_612189.2:n.29-728C=
NM_138316.4:c.29-728C=	NP_612189.2:n.29-728C=
NM_148977.2:c.704-728C=	NP_683878.1:n.704-728C=
NM_148978.2:c.29-728C=	NP_683879.1:n.29-728C=
NM_148978.3:c.29-728C=	NP_683879.1:n.29-728C=
ENST00000307534.8:c.704-728C=	ENSP00000302108.4:n.704-728C=
ENST00000322191.10:c.29-728C=	ENSP00000318526.6:n.29-728C=
ENST00000342512.3:c.29-728C=	ENSP00000345118.3:n.29-728C=
ENST00000342512.4:c.29-728C=	ENSP00000345118.3:n.29-728C=
XM_005269902.2:c.704-728C=	XP_005269959.1:n.704-728C=
XM_017016333.2:c.110-728C=	XP_016871822.1:n.110-728C=
XM_017016334.1:c.74-728C=	XP_016871823.1:n.74-728C=
XM_017016335.1:c.23-728C=	XP_016871824.1:n.23-728C=
XM_017016336.1:c.17-728C=	XP_016871825.1:n.17-728C=
XM_017016337.1:c.-17-728C=	XP_016871826.1:n.-17-728C=
XM_024448040.1:c.23-728C=	XP_024303808.1:n.23-728C=
XM_024448041.1:c.23-728C=	XP_024303809.1:n.23-728C=