Canonical Allele Identifier: CA1481090043

Gene: BANK1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101818625_101818626delinsAG , CM000666.2:g.101818625_101818626delinsAG	GRCh38
NC_000004.11:g.102739782_102739783delinsAG , CM000666.1:g.102739782_102739783delinsAG	GRCh37
NC_000004.10:g.102958805_102958806delinsAG	NCBI36
NG_015824.1:g.33019_33020delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322953.9:c.71-11183_71-11182delinsAG MANE Select	ENSP00000320509.4:n.71-11183_71-11182delinsAG
ENST00000322953.8:c.71-11183_71-11182delinsAG	ENSP00000320509.4:n.71-11183_71-11182delinsAG
ENST00000428908.5:c.70+27675_70+27676delinsAG	ENSP00000412748.1:n.70+27675_70+27676delinsAG
ENST00000444316.2:c.-21+4687_-21+4688delinsAG	ENSP00000388817.2:n.-21+4687_-21+4688delinsAG
ENST00000504592.5:c.26-11183_26-11182delinsAG	ENSP00000421443.1:n.26-11183_26-11182delinsAG
ENST00000508653.5:c.70+27675_70+27676delinsAG	ENSP00000422314.1:n.70+27675_70+27676delinsAG
NM_001083907.2:c.-21+4687_-21+4688delinsAG	NP_001077376.2:n.-21+4687_-21+4688delinsAG
NM_001127507.2:c.70+27675_70+27676delinsAG	NP_001120979.2:n.70+27675_70+27676delinsAG
NM_017935.4:c.71-11183_71-11182delinsAG	NP_060405.4:n.71-11183_71-11182delinsAG
XM_017008337.2:c.-20-11183_-20-11182delinsAG	XP_016863826.1:n.-20-11183_-20-11182delinsAG
NM_017935.5:c.71-11183_71-11182delinsAG MANE Select	NP_060405.5:n.71-11183_71-11182delinsAG
NM_001083907.3:c.-21+4687_-21+4688delinsAG	NP_001077376.3:n.-21+4687_-21+4688delinsAG
NM_001127507.3:c.70+27675_70+27676delinsAG	NP_001120979.3:n.70+27675_70+27676delinsAG