Canonical Allele Identifier: CA357951763

Gene: BANK1

Linked Data

• gnomAD v4: 4-101829822-A-C
• MyVariant Identifiers: chr4:g.102750979A>C (hg19) ; chr4:g.101829822A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101829822A>C , CM000666.2:g.101829822A>C	GRCh38
NC_000004.11:g.102750979A>C , CM000666.1:g.102750979A>C	GRCh37
NC_000004.10:g.102970002A>C	NCBI36
NG_015824.1:g.44216A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000322953.9:c.85A>C MANE Select	ENSP00000320509.4:p.Ile29Leu
ENST00000322953.8:c.85A>C	ENSP00000320509.4:p.Ile29Leu
ENST00000428908.5:c.71-25213A>C	ENSP00000412748.1:n.71-25213A>C
ENST00000444316.2:c.-6A>C	ENSP00000388817.2:n.-6A>C
ENST00000504592.5:c.40A>C	ENSP00000421443.1:p.Ile14Leu
ENST00000508653.5:c.71-25213A>C	ENSP00000422314.1:n.71-25213A>C
NM_001083907.2:c.-6A>C	NP_001077376.2:n.-6A>C
NM_001127507.2:c.71-25213A>C	NP_001120979.2:n.71-25213A>C
NM_017935.4:c.85A>C	NP_060405.4:p.Ile29Leu
XM_017008337.2:c.-6A>C	XP_016863826.1:n.-6A>C
NM_017935.5:c.85A>C MANE Select	NP_060405.5:p.Ile29Leu
NM_001083907.3:c.-6A>C	NP_001077376.3:n.-6A>C
NM_001127507.3:c.71-25213A>C	NP_001120979.3:n.71-25213A>C