Canonical Allele Identifier: CA517953208
Gene: SERPINA7 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.105277512A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.106033521A>T , CM000685.2:g.106033521A>T GRCh38
NC_000023.10:g.105277512A>T , CM000685.1:g.105277512A>T GRCh37
NC_000023.9:g.105164168A>T NCBI36
NG_021252.1:g.10207T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000372563.2:c.1227T>A MANE Select ENSP00000361644.1:p.Val409=
ENST00000327674.8:c.1227T>A ENSP00000329374.4:p.Val409=
ENST00000372563.1:c.1227T>A ENSP00000361644.1:p.Val409=
NM_000354.5:c.1227T>A NP_000345.2:p.Val409=
XM_006724683.1:c.1257T>A XP_006724746.1:p.Val419=
XM_005262180.4:c.*172T>A XP_005262237.1:n.*172T>A
XM_006724683.2:c.1257T>A XP_006724746.1:p.Val419=
NM_000354.6:c.1227T>A MANE Select NP_000345.2:p.Val409=