Canonical Allele Identifier: CA559376566

Gene: ANKRD55

Linked Data

• dbSNP Id: rs1348838426
• gnomAD v2: 5-55438867-G-A
• gnomAD v3: 5-56143040-G-A
• gnomAD v4: 5-56143040-G-A
• MyVariant Identifiers: chr5:g.55438867G>A (hg19) ; chr5:g.56143040G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56143040G>A , CM000667.2:g.56143040G>A	GRCh38
NC_000005.9:g.55438867G>A , CM000667.1:g.55438867G>A	GRCh37
NC_000005.8:g.55474624G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000341048.9:c.612+761C>T MANE Select	ENSP00000342295.4:n.612+761C>T
ENST00000341048.8:c.612+761C>T	ENSP00000342295.4:n.612+761C>T
ENST00000504958.6:c.484-15934C>T	ENSP00000424230.1:n.484-15934C>T
ENST00000505970.2:n.382+761C>T
NM_024669.2:c.612+761C>T	NP_078945.2:n.612+761C>T
XM_006714691.2:c.126+761C>T	XP_006714754.1:n.126+761C>T
XM_011543646.1:c.-65+761C>T	XP_011541948.1:n.-65+761C>T
XM_017009852.1:c.612+761C>T	XP_016865341.1:n.612+761C>T
XM_017009853.1:c.612+761C>T	XP_016865342.1:n.612+761C>T
XM_017009854.1:c.126+761C>T	XP_016865343.1:n.126+761C>T
NM_024669.3:c.612+761C>T MANE Select	NP_078945.2:n.612+761C>T