Canonical Allele Identifier: CA517953258
Gene: SERPINA7 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.105277599G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.106033608G>A , CM000685.2:g.106033608G>A GRCh38
NC_000023.10:g.105277599G>A , CM000685.1:g.105277599G>A GRCh37
NC_000023.9:g.105164255G>A NCBI36
NG_021252.1:g.10120C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000372563.2:c.1140C>T MANE Select ENSP00000361644.1:p.Phe380=
ENST00000327674.8:c.1140C>T ENSP00000329374.4:p.Phe380=
ENST00000372563.1:c.1140C>T ENSP00000361644.1:p.Phe380=
NM_000354.5:c.1140C>T NP_000345.2:p.Phe380=
XM_006724683.1:c.1170C>T XP_006724746.1:p.Phe390=
XM_005262180.4:c.*85C>T XP_005262237.1:n.*85C>T
XM_006724683.2:c.1170C>T XP_006724746.1:p.Phe390=
NM_000354.6:c.1140C>T MANE Select NP_000345.2:p.Phe380=