Canonical Allele Identifier: CA517953348
Gene: SERPINA7 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.105278250C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.106034259C>T , CM000685.2:g.106034259C>T GRCh38
NC_000023.10:g.105278250C>T , CM000685.1:g.105278250C>T GRCh37
NC_000023.9:g.105164906C>T NCBI36
NG_021252.1:g.9469G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000372563.2:c.1020G>A MANE Select ENSP00000361644.1:p.Glu340=
ENST00000327674.8:c.1020G>A ENSP00000329374.4:p.Glu340=
ENST00000372563.1:c.1020G>A ENSP00000361644.1:p.Glu340=
ENST00000487487.1:n.293G>A
NM_000354.5:c.1020G>A NP_000345.2:p.Glu340=
XM_005262180.3:c.1020G>A XP_005262237.1:p.Glu340=
XM_006724683.1:c.1020G>A XP_006724746.1:p.Glu340=
XM_005262180.4:c.1020G>A XP_005262237.1:p.Glu340=
XM_006724683.2:c.1020G>A XP_006724746.1:p.Glu340=
NM_000354.6:c.1020G>A MANE Select NP_000345.2:p.Glu340=