Canonical Allele Identifier: CA1481090014

Gene: BANK1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101818552_101818567delinsTCTGTGGTTTTGCTTC , CM000666.2:g.101818552_101818567delinsTCTGTGGTTTTGCTTC	GRCh38
NC_000004.11:g.102739709_102739724delinsTCTGTGGTTTTGCTTC , CM000666.1:g.102739709_102739724delinsTCTGTGGTTTTGCTTC	GRCh37
NC_000004.10:g.102958732_102958747delinsTCTGTGGTTTTGCTTC	NCBI36
NG_015824.1:g.32946_32961delinsTCTGTGGTTTTGCTTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000322953.9:c.71-11256_71-11241delinsTCTGTGGTTTTGCTTC MANE Select	ENSP00000320509.4:n.71-11256_71-11241deli...
ENST00000322953.8:c.71-11256_71-11241delinsTCTGTGGTTTTGCTTC	ENSP00000320509.4:n.71-11256_71-11241deli...
ENST00000428908.5:c.70+27602_70+27617delinsTCTGTGGTTTTGCTTC	ENSP00000412748.1:n.70+27602_70+27617deli...
ENST00000444316.2:c.-21+4614_-21+4629delinsTCTGTGGTTTTGCTTC	ENSP00000388817.2:n.-21+4614_-21+4629deli...
ENST00000504592.5:c.26-11256_26-11241delinsTCTGTGGTTTTGCTTC	ENSP00000421443.1:n.26-11256_26-11241deli...
ENST00000508653.5:c.70+27602_70+27617delinsTCTGTGGTTTTGCTTC	ENSP00000422314.1:n.70+27602_70+27617deli...
NM_001083907.2:c.-21+4614_-21+4629delinsTCTGTGGTTTTGCTTC	NP_001077376.2:n.-21+4614_-21+4629delinsT...
NM_001127507.2:c.70+27602_70+27617delinsTCTGTGGTTTTGCTTC	NP_001120979.2:n.70+27602_70+27617delinsT...
NM_017935.4:c.71-11256_71-11241delinsTCTGTGGTTTTGCTTC	NP_060405.4:n.71-11256_71-11241delinsTCTG...
XM_017008337.2:c.-20-11256_-20-11241delinsTCTGTGGTTTTGCTTC	XP_016863826.1:n.-20-11256_-20-11241delin...
NM_017935.5:c.71-11256_71-11241delinsTCTGTGGTTTTGCTTC MANE Select	NP_060405.5:n.71-11256_71-11241delinsTCTG...
NM_001083907.3:c.-21+4614_-21+4629delinsTCTGTGGTTTTGCTTC	NP_001077376.3:n.-21+4614_-21+4629delinsT...
NM_001127507.3:c.70+27602_70+27617delinsTCTGTGGTTTTGCTTC	NP_001120979.3:n.70+27602_70+27617delinsT...