Canonical Allele Identifier: CA517953216
Gene: SERPINA7 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.105277524A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.106033533A>G , CM000685.2:g.106033533A>G GRCh38
NC_000023.10:g.105277524A>G , CM000685.1:g.105277524A>G GRCh37
NC_000023.9:g.105164180A>G NCBI36
NG_021252.1:g.10195T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000372563.2:c.1215T>C MANE Select ENSP00000361644.1:p.Phe405=
ENST00000327674.8:c.1215T>C ENSP00000329374.4:p.Phe405=
ENST00000372563.1:c.1215T>C ENSP00000361644.1:p.Phe405=
NM_000354.5:c.1215T>C NP_000345.2:p.Phe405=
XM_006724683.1:c.1245T>C XP_006724746.1:p.Phe415=
XM_005262180.4:c.*160T>C XP_005262237.1:n.*160T>C
XM_006724683.2:c.1245T>C XP_006724746.1:p.Phe415=
NM_000354.6:c.1215T>C MANE Select NP_000345.2:p.Phe405=