Canonical Allele Identifier: CA1066075910

Gene: BANK1

Linked Data

• gnomAD v3: 4-101818894-T-TTTTTTTTTTTTTA
• gnomAD v4: 4-101818894-T-TTTTTTTTTTTTTA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101818895_101818896insTTTTTTTTTTTAT , CM000666.2:g.101818895_101818896insTTTTTTTTTTTAT	GRCh38
NC_000004.11:g.102740052_102740053insTTTTTTTTTTTAT , CM000666.1:g.102740052_102740053insTTTTTTTTTTTAT	GRCh37
NC_000004.10:g.102959075_102959076insTTTTTTTTTTTAT	NCBI36
NG_015824.1:g.33289_33290insTTTTTTTTTTTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322953.9:c.71-10913_71-10912insTTTTTTTTTTTAT MANE Select	ENSP00000320509.4:n.71-10913_71-10912insTTTTTTTTTTTAT
ENST00000322953.8:c.71-10913_71-10912insTTTTTTTTTTTAT	ENSP00000320509.4:n.71-10913_71-10912insTTTTTTTTTTTAT
ENST00000428908.5:c.70+27945_70+27946insTTTTTTTTTTTAT	ENSP00000412748.1:n.70+27945_70+27946insTTTTTTTTTTTAT
ENST00000444316.2:c.-21+4957_-21+4958insTTTTTTTTTTTAT	ENSP00000388817.2:n.-21+4957_-21+4958insTTTTTTTTTTTAT
ENST00000504592.5:c.26-10913_26-10912insTTTTTTTTTTTAT	ENSP00000421443.1:n.26-10913_26-10912insTTTTTTTTTTTAT
ENST00000508653.5:c.70+27945_70+27946insTTTTTTTTTTTAT	ENSP00000422314.1:n.70+27945_70+27946insTTTTTTTTTTTAT
NM_001083907.2:c.-21+4957_-21+4958insTTTTTTTTTTTAT	NP_001077376.2:n.-21+4957_-21+4958insTTTTTTTTTTTAT
NM_001127507.2:c.70+27945_70+27946insTTTTTTTTTTTAT	NP_001120979.2:n.70+27945_70+27946insTTTTTTTTTTTAT
NM_017935.4:c.71-10913_71-10912insTTTTTTTTTTTAT	NP_060405.4:n.71-10913_71-10912insTTTTTTTTTTTAT
XM_017008337.2:c.-20-10913_-20-10912insTTTTTTTTTTTAT	XP_016863826.1:n.-20-10913_-20-10912insTTTTTTTTTTTAT
NM_017935.5:c.71-10913_71-10912insTTTTTTTTTTTAT MANE Select	NP_060405.5:n.71-10913_71-10912insTTTTTTTTTTTAT
NM_001083907.3:c.-21+4957_-21+4958insTTTTTTTTTTTAT	NP_001077376.3:n.-21+4957_-21+4958insTTTTTTTTTTTAT
NM_001127507.3:c.70+27945_70+27946insTTTTTTTTTTTAT	NP_001120979.3:n.70+27945_70+27946insTTTTTTTTTTTAT