Canonical Allele Identifier: CA517953325
Gene: SERPINA7 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.105277689G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.106033698G>C , CM000685.2:g.106033698G>C GRCh38
NC_000023.10:g.105277689G>C , CM000685.1:g.105277689G>C GRCh37
NC_000023.9:g.105164345G>C NCBI36
NG_021252.1:g.10030C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000372563.2:c.1050C>G MANE Select ENSP00000361644.1:p.Ala350=
ENST00000327674.8:c.1050C>G ENSP00000329374.4:p.Ala350=
ENST00000372563.1:c.1050C>G ENSP00000361644.1:p.Ala350=
ENST00000487487.1:n.384C>G
NM_000354.5:c.1050C>G NP_000345.2:p.Ala350=
XM_005262180.3:c.1111C>G XP_005262237.1:p.Pro371Ala
XM_006724683.1:c.1080C>G XP_006724746.1:p.Ala360=
XM_005262180.4:c.1111C>G XP_005262237.1:p.Pro371Ala
XM_006724683.2:c.1080C>G XP_006724746.1:p.Ala360=
NM_000354.6:c.1050C>G MANE Select NP_000345.2:p.Ala350=