Canonical Allele Identifier: CA2610264128

Gene: CYP2C19

Linked Data

• gnomAD v4: 10-94775771-T-TCTG

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94775771_94775772insCTG , CM000672.2:g.94775771_94775772insCTG	GRCh38
NC_000010.10:g.96535528_96535529insCTG , CM000672.1:g.96535528_96535529insCTG	GRCh37
NC_000010.9:g.96525518_96525519insCTG	NCBI36
NG_008384.2:g.18066_18067insCTG
NG_008384.3:g.18091_18092insCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.481+232_481+233insCTG MANE Select	ENSP00000360372.3:n.481+232_481+233insCTG
ENST00000645461.1:n.1534+232_1534+233insCTG
ENST00000371321.7:c.481+232_481+233insCTG	ENSP00000360372.3:n.481+232_481+233insCTG
ENST00000464755.1:c.1244+232_1244+233insCTG	ENSP00000483243.1:n.1244+232_1244+233insCTG
ENST00000480405.2:c.*224_*225insCTG	ENSP00000483847.1:n.*224_*225insCTG
NM_000769.2:c.481+232_481+233insCTG	NP_000760.1:n.481+232_481+233insCTG
NM_000769.4:c.481+232_481+233insCTG MANE Select	NP_000760.1:n.481+232_481+233insCTG