Canonical Allele Identifier: CA1805111239

Gene: POP1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.98148607G= , CM000670.2:g.98148607G=	GRCh38
NC_000008.10:g.99160835G= , CM000670.1:g.99160835G=	GRCh37
NC_000008.9:g.99230011G=	NCBI36
NG_052869.1:g.36315G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000401707.7:c.1711-208G= MANE Select	ENSP00000385787.2:n.1711-208G=
ENST00000349693.3:c.1711-208G=	ENSP00000339529.3:n.1711-208G=
ENST00000401707.6:c.1711-208G=	ENSP00000385787.2:n.1711-208G=
NM_001145860.1:c.1711-208G=	NP_001139332.1:n.1711-208G=
NM_001145861.1:c.1711-208G=	NP_001139333.1:n.1711-208G=
NM_015029.2:c.1711-208G=	NP_055844.2:n.1711-208G=
XM_011516800.1:c.1711-208G=	XP_011515102.1:n.1711-208G=
NM_001145860.2:c.1711-208G= MANE Select	NP_001139332.1:n.1711-208G=
NM_001145861.2:c.1711-208G=	NP_001139333.1:n.1711-208G=
NM_015029.3:c.1711-208G=	NP_055844.2:n.1711-208G=