Canonical Allele Identifier: CA1963724294

Gene: PAMR1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.35489381G= , CM000673.2:g.35489381G=	GRCh38
NC_000011.9:g.35510929G= , CM000673.1:g.35510929G=	GRCh37
NC_000011.8:g.35467505G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000619888.5:c.379+2664C= MANE Select	ENSP00000483703.1:n.379+2664C=
ENST00000527605.5:c.259+2664C=	ENSP00000432591.1:n.259+2664C=
ENST00000529303.1:c.379+2664C=	ENSP00000433024.1:n.379+2664C=
ENST00000534803.1:n.391+2664C=
ENST00000611014.4:c.-532+2664C=	ENSP00000478867.1:n.-532+2664C=
ENST00000615849.4:c.379+2664C=	ENSP00000479260.1:n.379+2664C=
ENST00000619888.4:c.379+2664C=	ENSP00000483703.1:n.379+2664C=
ENST00000621476.4:c.259+2664C=	ENSP00000480961.1:n.259+2664C=
ENST00000622144.4:c.379+2664C=	ENSP00000482899.1:n.379+2664C=
NM_001001991.2:c.379+2664C=	NP_001001991.1:n.379+2664C=
NM_001282675.1:c.259+2664C=	NP_001269604.1:n.259+2664C=
NM_001282676.1:c.379+2664C=	NP_001269605.1:n.379+2664C=
NM_015430.3:c.379+2664C=	NP_056245.2:n.379+2664C=
NM_001001991.3:c.379+2664C= MANE Select	NP_001001991.1:n.379+2664C=
NM_015430.4:c.379+2664C=	NP_056245.2:n.379+2664C=
NM_001282675.2:c.259+2664C=	NP_001269604.1:n.259+2664C=
NM_001282676.2:c.379+2664C=	NP_001269605.1:n.379+2664C=