Canonical Allele Identifier: CA312389489

Gene: SEC23B

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.18511518_18511519del , CM000682.2:g.18511518_18511519del	GRCh38
NC_000020.10:g.18492162_18492163del , CM000682.1:g.18492162_18492163del	GRCh37
NC_000020.9:g.18440162_18440163del	NCBI36
NG_016281.1:g.8975_8976del
NG_016281.2:g.9037_9038del

Transcript Alleles

HGVS	Amino-acid Change
NM_006363.6:c.221+462_221+463del MANE Select	NP_006354.2:n.221+462_221+463del
ENST00000650089.1:c.221+462_221+463del MANE Select	ENSP00000497473.1:n.221+462_221+463del
NM_001172745.1:c.221+462_221+463del	NP_001166216.1:n.221+462_221+463del
NM_001172745.2:c.221+462_221+463del	NP_001166216.1:n.221+462_221+463del
NM_001172745.3:c.221+462_221+463del	NP_001166216.1:n.221+462_221+463del
NM_001172746.1:c.221+462_221+463del	NP_001166217.1:n.221+462_221+463del
NM_001172746.2:c.221+462_221+463del	NP_001166217.1:n.221+462_221+463del
NM_001172746.3:c.221+462_221+463del	NP_001166217.1:n.221+462_221+463del
NM_006363.4:c.221+462_221+463del	NP_006354.2:n.221+462_221+463del
NM_032985.4:c.221+462_221+463del	NP_116780.1:n.221+462_221+463del
NM_032985.5:c.221+462_221+463del	NP_116780.1:n.221+462_221+463del
NM_032985.6:c.221+462_221+463del	NP_116780.1:n.221+462_221+463del
NM_032986.3:c.221+462_221+463del	NP_116781.1:n.221+462_221+463del
NM_032986.4:c.221+462_221+463del	NP_116781.1:n.221+462_221+463del
NM_032986.5:c.221+462_221+463del	NP_116781.1:n.221+462_221+463del
ENST00000262544.6:c.221+462_221+463del	ENSP00000262544.2:n.221+462_221+463del
ENST00000336714.7:c.221+462_221+463del	ENSP00000338844.3:n.221+462_221+463del
ENST00000336714.8:c.221+462_221+463del	ENSP00000338844.3:n.221+462_221+463del
ENST00000377465.5:c.221+462_221+463del	ENSP00000366685.1:n.221+462_221+463del
ENST00000377465.6:c.221+462_221+463del	ENSP00000366685.1:n.221+462_221+463del
ENST00000377475.7:c.221+462_221+463del	ENSP00000366695.3:n.221+462_221+463del
ENST00000450074.5:c.221+462_221+463del	ENSP00000403971.1:n.221+462_221+463del
ENST00000450074.6:c.221+462_221+463del	ENSP00000403971.1:n.221+462_221+463del
ENST00000494645.1:n.80+462_80+463del
ENST00000643747.1:c.221+462_221+463del	ENSP00000496460.1:n.221+462_221+463del
XM_017027593.1:c.221+462_221+463del	XP_016883082.1:n.221+462_221+463del