Canonical Allele Identifier: CA553732474

Gene: BANK1

Linked Data

• dbSNP Id: rs1297919186
• gnomAD v2: 4-102838881-A-T
• MyVariant Identifiers: chr4:g.102838881A>T (hg19) ; chr4:g.101917724A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101917724A>T , CM000666.2:g.101917724A>T	GRCh38
NC_000004.11:g.102838881A>T , CM000666.1:g.102838881A>T	GRCh37
NC_000004.10:g.103057904A>T	NCBI36
NG_015824.1:g.132118A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322953.9:c.1010-269A>T MANE Select	ENSP00000320509.4:n.1010-269A>T
ENST00000322953.8:c.1010-269A>T	ENSP00000320509.4:n.1010-269A>T
ENST00000428908.5:c.611-269A>T	ENSP00000412748.1:n.611-269A>T
ENST00000444316.2:c.920-269A>T	ENSP00000388817.2:n.920-269A>T
ENST00000504592.5:c.965-269A>T	ENSP00000421443.1:n.965-269A>T
ENST00000508653.5:c.611-269A>T	ENSP00000422314.1:n.611-269A>T
NM_001083907.2:c.920-269A>T	NP_001077376.2:n.920-269A>T
NM_001127507.2:c.611-269A>T	NP_001120979.2:n.611-269A>T
NM_017935.4:c.1010-269A>T	NP_060405.4:n.1010-269A>T
XM_017008337.2:c.920-269A>T	XP_016863826.1:n.920-269A>T
NM_017935.5:c.1010-269A>T MANE Select	NP_060405.5:n.1010-269A>T
NM_001083907.3:c.920-269A>T	NP_001077376.3:n.920-269A>T
NM_001127507.3:c.611-269A>T	NP_001120979.3:n.611-269A>T