Canonical Allele Identifier: CA2578154637

Gene: BANK1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101918018del , CM000666.2:g.101918018del	GRCh38
NC_000004.11:g.102839175del , CM000666.1:g.102839175del	GRCh37
NC_000004.10:g.103058198del	NCBI36
NG_015824.1:g.132412del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322953.9:c.1035del MANE Select	ENSP00000320509.4:p.Leu346PhefsTer10
ENST00000322953.8:c.1035del	ENSP00000320509.4:p.Leu346PhefsTer10
ENST00000428908.5:c.636del	ENSP00000412748.1:p.Leu213PhefsTer10
ENST00000444316.2:c.945del	ENSP00000388817.2:p.Leu316PhefsTer10
ENST00000504592.5:c.990del	ENSP00000421443.1:p.Leu331PhefsTer10
ENST00000508653.5:c.636del	ENSP00000422314.1:p.Leu213PhefsTer10
NM_001083907.2:c.945del	NP_001077376.2:p.Leu316PhefsTer10
NM_001127507.2:c.636del	NP_001120979.2:p.Leu213PhefsTer10
NM_017935.4:c.1035del	NP_060405.4:p.Leu346PhefsTer10
XM_017008337.2:c.945del	XP_016863826.1:p.Leu316PhefsTer10
NM_017935.5:c.1035del MANE Select	NP_060405.5:p.Leu346PhefsTer10
NM_001083907.3:c.945del	NP_001077376.3:p.Leu316PhefsTer10
NM_001127507.3:c.636del	NP_001120979.3:p.Leu213PhefsTer10