Canonical Allele Identifier: CA518103389
Gene: SERPINA7 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.105280492C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.106036501C>A , CM000685.2:g.106036501C>A GRCh38
NC_000023.10:g.105280492C>A , CM000685.1:g.105280492C>A GRCh37
NC_000023.9:g.105167148C>A NCBI36
NG_021252.1:g.7227G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000372563.2:c.558G>T MANE Select ENSP00000361644.1:p.Val186=
ENST00000327674.8:c.558G>T ENSP00000329374.4:p.Val186=
ENST00000372563.1:c.558G>T ENSP00000361644.1:p.Val186=
NM_000354.5:c.558G>T NP_000345.2:p.Val186=
XM_005262180.3:c.558G>T XP_005262237.1:p.Val186=
XM_006724683.1:c.558G>T XP_006724746.1:p.Val186=
XM_005262180.4:c.558G>T XP_005262237.1:p.Val186=
XM_006724683.2:c.558G>T XP_006724746.1:p.Val186=
NM_000354.6:c.558G>T MANE Select NP_000345.2:p.Val186=