Canonical Allele Identifier: CA1926899651

Gene: PANK1

Linked Data

• dbSNP Id: rs11185777

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89594453G>C , CM000672.2:g.89594453G>C	GRCh38
NC_000010.10:g.91354210G>C , CM000672.1:g.91354210G>C	GRCh37
NC_000010.9:g.91344190G>C	NCBI36
NG_029474.1:g.56120C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000342512.4:c.636-464C>G	ENSP00000345118.3:n.636-464C>G
ENST00000307534.10:c.900-464C>G MANE Select	ENSP00000302108.5:n.900-464C>G
ENST00000307534.8:c.1311-464C>G	ENSP00000302108.4:n.1311-464C>G
ENST00000322191.10:c.636-1133C>G	ENSP00000318526.6:n.636-1133C>G
ENST00000342512.3:c.636-464C>G	ENSP00000345118.3:n.636-464C>G
NM_138316.3:c.636-1133C>G	NP_612189.2:n.636-1133C>G
NM_148977.2:c.1311-464C>G	NP_683878.1:n.1311-464C>G
NM_148978.2:c.636-464C>G	NP_683879.1:n.636-464C>G
XM_005269902.2:c.1311-1133C>G	XP_005269959.1:n.1311-1133C>G
XM_017016333.2:c.717-464C>G	XP_016871822.1:n.717-464C>G
XM_017016334.1:c.681-464C>G	XP_016871823.1:n.681-464C>G
XM_017016335.1:c.630-464C>G	XP_016871824.1:n.630-464C>G
XM_017016336.1:c.624-464C>G	XP_016871825.1:n.624-464C>G
XM_017016337.1:c.591-464C>G	XP_016871826.1:n.591-464C>G
XM_017016338.1:c.-254C>G	XP_016871827.1:n.-254C>G
XM_024448040.1:c.630-464C>G	XP_024303808.1:n.630-464C>G
XM_024448041.1:c.630-464C>G	XP_024303809.1:n.630-464C>G
NM_138316.4:c.636-1133C>G	NP_612189.2:n.636-1133C>G
NM_148978.3:c.636-464C>G	NP_683879.1:n.636-464C>G
NM_148977.3:c.900-464C>G MANE Select	NP_683878.2:n.900-464C>G