Canonical Allele Identifier: CA1978712965

Gene: CCDC88B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64340263G>T , CM000673.2:g.64340263G>T	GRCh38
NC_000011.9:g.64107735G>T , CM000673.1:g.64107735G>T	GRCh37
NC_000011.8:g.63864311G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356786.10:c.-4G>T MANE Select	ENSP00000349238.5:n.-4G>T
ENST00000356786.9:c.-4G>T	ENSP00000349238.5:n.-4G>T
ENST00000463837.5:n.41G>T
NM_032251.5:c.-4G>T	NP_115627.6:n.-4G>T
XM_006718519.2:c.-4G>T	XP_006718582.1:n.-4G>T
XM_011544957.1:c.-4G>T	XP_011543259.1:n.-4G>T
XM_011544958.1:c.-4G>T	XP_011543260.1:n.-4G>T
XM_011544959.1:c.-4G>T	XP_011543261.1:n.-4G>T
XM_011544960.1:c.-4G>T	XP_011543262.1:n.-4G>T
XM_011544961.1:c.-4G>T	XP_011543263.1:n.-4G>T
XR_428944.2:n.86-185C>A
XR_949893.1:n.66G>T
XR_949894.1:n.67G>T
XM_006718519.4:c.-4G>T	XP_006718582.1:n.-4G>T
XM_011544957.2:c.-4G>T	XP_011543259.1:n.-4G>T
XM_011544959.2:c.-4G>T	XP_011543261.1:n.-4G>T
XM_011544960.2:c.-4G>T	XP_011543262.1:n.-4G>T
XM_017017601.1:c.-4G>T	XP_016873090.1:n.-4G>T
XM_024448450.1:c.-4G>T	XP_024304218.1:n.-4G>T
XM_024448451.1:c.-4G>T	XP_024304219.1:n.-4G>T
XR_002957140.1:n.59G>T
XR_428944.3:n.102-185C>A
XR_949893.3:n.60G>T
XR_949894.3:n.60G>T
NM_032251.6:c.-4G>T MANE Select	NP_115627.6:n.-4G>T