Canonical Allele Identifier: CA784480725

Gene: BANK1

Linked Data

• dbSNP Id: rs1425058255
• MyVariant Identifiers: chr4:g.102740032_102740033insA (hg19) ; chr4:g.101818875_101818876insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101818875_101818876insA , CM000666.2:g.101818875_101818876insA	GRCh38
NC_000004.11:g.102740032_102740033insA , CM000666.1:g.102740032_102740033insA	GRCh37
NC_000004.10:g.102959055_102959056insA	NCBI36
NG_015824.1:g.33269_33270insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322953.9:c.71-10933_71-10932insA MANE Select	ENSP00000320509.4:n.71-10933_71-10932insA
ENST00000322953.8:c.71-10933_71-10932insA	ENSP00000320509.4:n.71-10933_71-10932insA
ENST00000428908.5:c.70+27925_70+27926insA	ENSP00000412748.1:n.70+27925_70+27926insA
ENST00000444316.2:c.-21+4937_-21+4938insA	ENSP00000388817.2:n.-21+4937_-21+4938insA
ENST00000504592.5:c.26-10933_26-10932insA	ENSP00000421443.1:n.26-10933_26-10932insA
ENST00000508653.5:c.70+27925_70+27926insA	ENSP00000422314.1:n.70+27925_70+27926insA
NM_001083907.2:c.-21+4937_-21+4938insA	NP_001077376.2:n.-21+4937_-21+4938insA
NM_001127507.2:c.70+27925_70+27926insA	NP_001120979.2:n.70+27925_70+27926insA
NM_017935.4:c.71-10933_71-10932insA	NP_060405.4:n.71-10933_71-10932insA
XM_017008337.2:c.-20-10933_-20-10932insA	XP_016863826.1:n.-20-10933_-20-10932insA
NM_017935.5:c.71-10933_71-10932insA MANE Select	NP_060405.5:n.71-10933_71-10932insA
NM_001083907.3:c.-21+4937_-21+4938insA	NP_001077376.3:n.-21+4937_-21+4938insA
NM_001127507.3:c.70+27925_70+27926insA	NP_001120979.3:n.70+27925_70+27926insA