Canonical Allele Identifier: CA917265057

Gene: BANK1

Linked Data

• dbSNP Id: rs1578341864

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101829808_101829809insTTTTT , CM000666.2:g.101829808_101829809insTTTTT	GRCh38
NC_000004.11:g.102750965_102750966insTTTTT , CM000666.1:g.102750965_102750966insTTTTT	GRCh37
NC_000004.10:g.102969988_102969989insTTTTT	NCBI36
NG_015824.1:g.44202_44203insTTTTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000322953.9:c.71_72insTTTTT MANE Select	ENSP00000320509.4:p.Asn25PhefsTer2
ENST00000322953.8:c.71_72insTTTTT	ENSP00000320509.4:p.Asn25PhefsTer2
ENST00000428908.5:c.71-25227_71-25226insTTTTT	ENSP00000412748.1:n.71-25227_71-25226insT...
ENST00000444316.2:c.-20_-19insTTTTT	ENSP00000388817.2:n.-20_-19insTTTTT
ENST00000504592.5:c.26_27insTTTTT	ENSP00000421443.1:p.Asn10PhefsTer2
ENST00000508653.5:c.71-25227_71-25226insTTTTT	ENSP00000422314.1:n.71-25227_71-25226insT...
NM_001083907.2:c.-20_-19insTTTTT	NP_001077376.2:n.-20_-19insTTTTT
NM_001127507.2:c.71-25227_71-25226insTTTTT	NP_001120979.2:n.71-25227_71-25226insTTTT...
NM_017935.4:c.71_72insTTTTT	NP_060405.4:p.Asn25PhefsTer2
XM_017008337.2:c.-20_-19insTTTTT	XP_016863826.1:n.-20_-19insTTTTT
NM_017935.5:c.71_72insTTTTT MANE Select	NP_060405.5:p.Asn25PhefsTer2
NM_001083907.3:c.-20_-19insTTTTT	NP_001077376.3:n.-20_-19insTTTTT
NM_001127507.3:c.71-25227_71-25226insTTTTT	NP_001120979.3:n.71-25227_71-25226insTTTT...