Canonical Allele Identifier: CA357956195

Gene: BANK1

Linked Data

• gnomAD v4: 4-101918094-G-C
• MyVariant Identifiers: chr4:g.102839251G>C (hg19) ; chr4:g.101918094G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101918094G>C , CM000666.2:g.101918094G>C	GRCh38
NC_000004.11:g.102839251G>C , CM000666.1:g.102839251G>C	GRCh37
NC_000004.10:g.103058274G>C	NCBI36
NG_015824.1:g.132488G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322953.9:c.1111G>C MANE Select	ENSP00000320509.4:p.Ala371Pro
ENST00000322953.8:c.1111G>C	ENSP00000320509.4:p.Ala371Pro
ENST00000428908.5:c.712G>C	ENSP00000412748.1:p.Ala238Pro
ENST00000444316.2:c.1021G>C	ENSP00000388817.2:p.Ala341Pro
ENST00000504592.5:c.1066G>C	ENSP00000421443.1:p.Ala356Pro
ENST00000508653.5:c.712G>C	ENSP00000422314.1:p.Ala238Pro
NM_001083907.2:c.1021G>C	NP_001077376.2:p.Ala341Pro
NM_001127507.2:c.712G>C	NP_001120979.2:p.Ala238Pro
NM_017935.4:c.1111G>C	NP_060405.4:p.Ala371Pro
XM_017008337.2:c.1021G>C	XP_016863826.1:p.Ala341Pro
NM_017935.5:c.1111G>C MANE Select	NP_060405.5:p.Ala371Pro
NM_001083907.3:c.1021G>C	NP_001077376.3:p.Ala341Pro
NM_001127507.3:c.712G>C	NP_001120979.3:p.Ala238Pro