Canonical Allele Identifier: CA517953331
Gene: SERPINA7 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.105278221C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.106034230C>A , CM000685.2:g.106034230C>A GRCh38
NC_000023.10:g.105278221C>A , CM000685.1:g.105278221C>A GRCh37
NC_000023.9:g.105164877C>A NCBI36
NG_021252.1:g.9498G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372563.2:c.1044+5G>T MANE Select ENSP00000361644.1:n.1044+5G>T
ENST00000327674.8:c.1044+5G>T ENSP00000329374.4:n.1044+5G>T
ENST00000372563.1:c.1044+5G>T ENSP00000361644.1:n.1044+5G>T
ENST00000487487.1:n.317+5G>T
NM_000354.5:c.1044+5G>T NP_000345.2:n.1044+5G>T
XM_005262180.3:c.1044+5G>T XP_005262237.1:n.1044+5G>T
XM_006724683.1:c.1044+5G>T XP_006724746.1:n.1044+5G>T
XM_005262180.4:c.1044+5G>T XP_005262237.1:n.1044+5G>T
XM_006724683.2:c.1044+5G>T XP_006724746.1:n.1044+5G>T
NM_000354.6:c.1044+5G>T MANE Select NP_000345.2:n.1044+5G>T