Canonical Allele Identifier: CA440603687

Gene: BANK1

Linked Data

• MyVariant Identifiers: chr4:g.102740027del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101818870del , CM000666.2:g.101818870del	GRCh38
NC_000004.11:g.102740027del , CM000666.1:g.102740027del	GRCh37
NC_000004.10:g.102959050del	NCBI36
NG_015824.1:g.33264del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322953.9:c.71-10938del MANE Select	ENSP00000320509.4:n.71-10938del
ENST00000322953.8:c.71-10938del	ENSP00000320509.4:n.71-10938del
ENST00000428908.5:c.70+27920del	ENSP00000412748.1:n.70+27920del
ENST00000444316.2:c.-21+4932del	ENSP00000388817.2:n.-21+4932del
ENST00000504592.5:c.26-10938del	ENSP00000421443.1:n.26-10938del
ENST00000508653.5:c.70+27920del	ENSP00000422314.1:n.70+27920del
NM_001083907.2:c.-21+4932del	NP_001077376.2:n.-21+4932del
NM_001127507.2:c.70+27920del	NP_001120979.2:n.70+27920del
NM_017935.4:c.71-10938del	NP_060405.4:n.71-10938del
XM_017008337.2:c.-20-10938del	XP_016863826.1:n.-20-10938del
NM_017935.5:c.71-10938del MANE Select	NP_060405.5:n.71-10938del
NM_001083907.3:c.-21+4932del	NP_001077376.3:n.-21+4932del
NM_001127507.3:c.70+27920del	NP_001120979.3:n.70+27920del