Canonical Allele Identifier: CA103059594

Gene: BANK1

Linked Data

• dbSNP Id: rs974998530
• MyVariant Identifiers: chr4:g.102739788_102739791del (hg19) ; chr4:g.101818631_101818634del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101818634_101818637del , CM000666.2:g.101818634_101818637del	GRCh38
NC_000004.11:g.102739791_102739794del , CM000666.1:g.102739791_102739794del	GRCh37
NC_000004.10:g.102958814_102958817del	NCBI36
NG_015824.1:g.33028_33031del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322953.9:c.71-11174_71-11171del MANE Select	ENSP00000320509.4:n.71-11174_71-11171del
ENST00000322953.8:c.71-11174_71-11171del	ENSP00000320509.4:n.71-11174_71-11171del
ENST00000428908.5:c.70+27684_70+27687del	ENSP00000412748.1:n.70+27684_70+27687del
ENST00000444316.2:c.-21+4696_-21+4699del	ENSP00000388817.2:n.-21+4696_-21+4699del
ENST00000504592.5:c.26-11174_26-11171del	ENSP00000421443.1:n.26-11174_26-11171del
ENST00000508653.5:c.70+27684_70+27687del	ENSP00000422314.1:n.70+27684_70+27687del
NM_001083907.2:c.-21+4696_-21+4699del	NP_001077376.2:n.-21+4696_-21+4699del
NM_001127507.2:c.70+27684_70+27687del	NP_001120979.2:n.70+27684_70+27687del
NM_017935.4:c.71-11174_71-11171del	NP_060405.4:n.71-11174_71-11171del
XM_017008337.2:c.-20-11174_-20-11171del	XP_016863826.1:n.-20-11174_-20-11171del
NM_017935.5:c.71-11174_71-11171del MANE Select	NP_060405.5:n.71-11174_71-11171del
NM_001083907.3:c.-21+4696_-21+4699del	NP_001077376.3:n.-21+4696_-21+4699del
NM_001127507.3:c.70+27684_70+27687del	NP_001120979.3:n.70+27684_70+27687del