Canonical Allele Identifier: CA1066075895

Gene: BANK1

Linked Data

• gnomAD v3: 4-101818892-G-GTTTTTTT
• gnomAD v4: 4-101818892-G-GTTTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101818895_101818896insTTTTTTT , CM000666.2:g.101818895_101818896insTTTTTTT	GRCh38
NC_000004.11:g.102740052_102740053insTTTTTTT , CM000666.1:g.102740052_102740053insTTTTTTT	GRCh37
NC_000004.10:g.102959075_102959076insTTTTTTT	NCBI36
NG_015824.1:g.33289_33290insTTTTTTT

Transcript Alleles

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