Canonical Allele Identifier: CA517953296
Gene: SERPINA7 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.105277647A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.106033656A>C , CM000685.2:g.106033656A>C GRCh38
NC_000023.10:g.105277647A>C , CM000685.1:g.105277647A>C GRCh37
NC_000023.9:g.105164303A>C NCBI36
NG_021252.1:g.10072T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000372563.2:c.1092T>G MANE Select ENSP00000361644.1:p.Ala364=
ENST00000327674.8:c.1092T>G ENSP00000329374.4:p.Ala364=
ENST00000372563.1:c.1092T>G ENSP00000361644.1:p.Ala364=
NM_000354.5:c.1092T>G NP_000345.2:p.Ala364=
XM_005262180.3:c.*37T>G XP_005262237.1:n.*37T>G
XM_006724683.1:c.1122T>G XP_006724746.1:p.Ala374=
XM_005262180.4:c.*37T>G XP_005262237.1:n.*37T>G
XM_006724683.2:c.1122T>G XP_006724746.1:p.Ala374=
NM_000354.6:c.1092T>G MANE Select NP_000345.2:p.Ala364=