Canonical Allele Identifier: CA2306501430

Gene: ALPK2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.58546158G= , CM000680.2:g.58546158G=	GRCh38
NC_000018.9:g.56213390G= , CM000680.1:g.56213390G=	GRCh37
NC_000018.8:g.54364370G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_052947.4:c.1963-7934C= MANE Select	NP_443179.3:n.1963-7934C=
ENST00000361673.4:c.1963-7934C= MANE Select	ENSP00000354991.3:n.1963-7934C=
NM_052947.3:c.1963-7934C=	NP_443179.3:n.1963-7934C=
ENST00000361673.3:c.1963-7934C=	ENSP00000354991.3:n.1963-7934C=
ENST00000587399.1:n.400-1483C=
ENST00000587842.1:n.212-940C=
XM_011525801.1:c.1963-7934C=	XP_011524103.1:n.1963-7934C=
XM_011525801.3:c.1963-7934C=	XP_011524103.1:n.1963-7934C=
XM_011525802.1:c.1681-7934C=	XP_011524104.1:n.1681-7934C=
XM_011525802.2:c.1681-7934C=	XP_011524104.1:n.1681-7934C=
XM_017025535.2:c.1963-7934C=	XP_016881024.1:n.1963-7934C=
XM_017025536.2:c.1963-7934C=	XP_016881025.1:n.1963-7934C=
XM_017025537.2:c.1963-7934C=	XP_016881026.1:n.1963-7934C=
XM_017025539.1:c.-45-7934C=	XP_016881028.1:n.-45-7934C=
XR_935194.1:n.2408-7934C=