Canonical Allele Identifier: CA869645898

Gene: SERPINA7

Linked Data

• dbSNP Id: rs1444922755
• gnomAD v3: X-106034093-CTG-C
• gnomAD v4: X-106034093-CTG-C
• MyVariant Identifiers: chrX:g.105278085_105278086del (hg19) ; chrX:g.106034094_106034095del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.106034094_106034095del , CM000685.2:g.106034094_106034095del	GRCh38
NC_000023.10:g.105278085_105278086del , CM000685.1:g.105278085_105278086del	GRCh37
NC_000023.9:g.105164741_105164742del	NCBI36
NG_021252.1:g.9633_9634del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372563.2:c.1044+140_1044+141del MANE Select	ENSP00000361644.1:n.1044+140_1044+141del
ENST00000327674.8:c.1044+140_1044+141del	ENSP00000329374.4:n.1044+140_1044+141del
ENST00000372563.1:c.1044+140_1044+141del	ENSP00000361644.1:n.1044+140_1044+141del
ENST00000487487.1:n.317+140_317+141del
NM_000354.5:c.1044+140_1044+141del	NP_000345.2:n.1044+140_1044+141del
XM_005262180.3:c.1044+140_1044+141del	XP_005262237.1:n.1044+140_1044+141del
XM_006724683.1:c.1044+140_1044+141del	XP_006724746.1:n.1044+140_1044+141del
XM_005262180.4:c.1044+140_1044+141del	XP_005262237.1:n.1044+140_1044+141del
XM_006724683.2:c.1044+140_1044+141del	XP_006724746.1:n.1044+140_1044+141del
NM_000354.6:c.1044+140_1044+141del MANE Select	NP_000345.2:n.1044+140_1044+141del