Canonical Allele Identifier: CA517953320

Gene: SERPINA7

Linked Data

• MyVariant Identifiers: chrX:g.105277680A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.106033689A>G , CM000685.2:g.106033689A>G	GRCh38
NC_000023.10:g.105277680A>G , CM000685.1:g.105277680A>G	GRCh37
NC_000023.9:g.105164336A>G	NCBI36
NG_021252.1:g.10039T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372563.2:c.1059T>C MANE Select	ENSP00000361644.1:p.Ala353=
ENST00000327674.8:c.1059T>C	ENSP00000329374.4:p.Ala353=
ENST00000372563.1:c.1059T>C	ENSP00000361644.1:p.Ala353=
ENST00000487487.1:n.393T>C
NM_000354.5:c.1059T>C	NP_000345.2:p.Ala353=
XM_005262180.3:c.*4T>C	XP_005262237.1:n.*4T>C
XM_006724683.1:c.1089T>C	XP_006724746.1:p.Ala363=
XM_005262180.4:c.*4T>C	XP_005262237.1:n.*4T>C
XM_006724683.2:c.1089T>C	XP_006724746.1:p.Ala363=
NM_000354.6:c.1059T>C MANE Select	NP_000345.2:p.Ala353=