Canonical Allele Identifier: CA710124201

Gene: SERPINA12

Linked Data

• dbSNP Id: rs11627075
• gnomAD v3: 14-94505905-C-T
• gnomAD v4: 14-94505905-C-T
• MyVariant Identifiers: chr14:g.94972242C>T (hg19) ; chr14:g.94505905C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.94505905C>T , CM000676.2:g.94505905C>T	GRCh38
NC_000014.8:g.94972242C>T , CM000676.1:g.94972242C>T	GRCh37
NC_000014.7:g.94041995C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000677451.1:c.-34+3437G>A MANE Select	ENSP00000503935.1:n.-34+3437G>A
ENST00000341228.2:c.-17-7491G>A	ENSP00000342109.2:n.-17-7491G>A
NM_173850.3:c.-17-7491G>A	NP_776249.1:n.-17-7491G>A
XM_011536451.1:c.-34+3437G>A	XP_011534753.1:n.-34+3437G>A
XM_011536454.1:c.-18+3437G>A	XP_011534756.1:n.-18+3437G>A
XM_011536451.3:c.-34+3437G>A	XP_011534753.1:n.-34+3437G>A
XM_011536454.3:c.-18+3437G>A	XP_011534756.1:n.-18+3437G>A
XM_017020989.2:c.-34+3442G>A	XP_016876478.1:n.-34+3442G>A
XM_017020990.1:c.-18+3442G>A	XP_016876479.1:n.-18+3442G>A
NM_173850.4:c.-17-7491G>A	NP_776249.1:n.-17-7491G>A
NM_001382267.1:c.-34+3437G>A MANE Select	NP_001369196.1:n.-34+3437G>A