Canonical Allele Identifier: CA2160461639

Gene: PPP1R13B

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.103753628_103753629delinsTA , CM000676.2:g.103753628_103753629delinsTA	GRCh38
NC_000014.8:g.104219965_104219966delinsTA , CM000676.1:g.104219965_104219966delinsTA	GRCh37
NC_000014.7:g.103289718_103289719delinsTA	NCBI36
NG_046915.1:g.100339_100340delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000202556.14:c.632-433_632-432delinsTA MANE Select	ENSP00000202556.9:n.632-433_632-432delinsTA
ENST00000647748.1:c.587-433_587-432delinsTA	ENSP00000497343.1:n.587-433_587-432delinsTA
ENST00000202556.13:c.632-433_632-432delinsTA	ENSP00000202556.9:n.632-433_632-432delinsTA
ENST00000556325.1:n.35-13566_35-13565delinsTA
ENST00000557082.5:c.*877-433_*877-432delinsTA	ENSP00000451396.1:n.*877-433_*877-432delinsTA
NM_015316.2:c.632-433_632-432delinsTA	NP_056131.2:n.632-433_632-432delinsTA
XM_005267487.3:c.836-433_836-432delinsTA	XP_005267544.1:n.836-433_836-432delinsTA
XM_011536592.1:c.836-433_836-432delinsTA	XP_011534894.1:n.836-433_836-432delinsTA
XM_011536593.1:c.836-433_836-432delinsTA	XP_011534895.1:n.836-433_836-432delinsTA
XM_011536594.1:c.836-433_836-432delinsTA	XP_011534896.1:n.836-433_836-432delinsTA
XM_011536595.1:c.632-433_632-432delinsTA	XP_011534897.1:n.632-433_632-432delinsTA
XM_011536596.1:c.623-433_623-432delinsTA	XP_011534898.1:n.623-433_623-432delinsTA
XM_011536597.1:c.623-433_623-432delinsTA	XP_011534899.1:n.623-433_623-432delinsTA
XR_245676.2:n.1319-433_1319-432delinsTA
XR_943410.1:n.1319-433_1319-432delinsTA
XR_943411.1:n.1319-433_1319-432delinsTA
XR_943412.1:n.1319-433_1319-432delinsTA
XR_943413.1:n.1319-433_1319-432delinsTA
XM_005267487.5:c.836-433_836-432delinsTA	XP_005267544.1:n.836-433_836-432delinsTA
XM_011536593.3:c.836-433_836-432delinsTA	XP_011534895.1:n.836-433_836-432delinsTA
XM_017021116.1:c.632-433_632-432delinsTA	XP_016876605.1:n.632-433_632-432delinsTA
XM_017021117.1:c.623-433_623-432delinsTA	XP_016876606.1:n.623-433_623-432delinsTA
XR_001750204.2:n.1679-433_1679-432delinsTA
XR_001750205.2:n.1679-433_1679-432delinsTA
XR_001750206.2:n.1679-433_1679-432delinsTA
XR_245676.4:n.1679-433_1679-432delinsTA
XR_943413.3:n.1679-433_1679-432delinsTA
NM_015316.3:c.632-433_632-432delinsTA MANE Select	NP_056131.2:n.632-433_632-432delinsTA