Canonical Allele Identifier: CA517953392
Gene: SERPINA7 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.105278316G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.106034325G>A , CM000685.2:g.106034325G>A GRCh38
NC_000023.10:g.105278316G>A , CM000685.1:g.105278316G>A GRCh37
NC_000023.9:g.105164972G>A NCBI36
NG_021252.1:g.9403C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372563.2:c.954C>T MANE Select ENSP00000361644.1:p.Ala318=
ENST00000327674.8:c.954C>T ENSP00000329374.4:p.Ala318=
ENST00000372563.1:c.954C>T ENSP00000361644.1:p.Ala318=
ENST00000487487.1:n.227C>T
NM_000354.5:c.954C>T NP_000345.2:p.Ala318=
XM_005262180.3:c.954C>T XP_005262237.1:p.Ala318=
XM_006724683.1:c.954C>T XP_006724746.1:p.Ala318=
XM_005262180.4:c.954C>T XP_005262237.1:p.Ala318=
XM_006724683.2:c.954C>T XP_006724746.1:p.Ala318=
NM_000354.6:c.954C>T MANE Select NP_000345.2:p.Ala318=