Canonical Allele Identifier: CA1929222212

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94781720_94781726delinsTTATTTA , CM000672.2:g.94781720_94781726delinsTTATTTA	GRCh38
NC_000010.10:g.96541477_96541483delinsTTATTTA , CM000672.1:g.96541477_96541483delinsTTATTTA	GRCh37
NC_000010.9:g.96531467_96531473delinsTTATTTA	NCBI36
NG_008384.2:g.24015_24021delinsTTATTTA
NG_008384.3:g.24040_24046delinsTTATTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.643-101_643-95delinsTTATTTA MANE Select	ENSP00000360372.3:n.643-101_643-95delinsTTATTTA
ENST00000645461.1:n.1696-101_1696-95delinsTTATTTA
ENST00000371321.7:c.643-101_643-95delinsTTATTTA	ENSP00000360372.3:n.643-101_643-95delinsTTATTTA
ENST00000464755.1:c.1406-101_1406-95delinsTTATTTA	ENSP00000483243.1:n.1406-101_1406-95delinsTTATTTA
NM_000769.2:c.643-101_643-95delinsTTATTTA	NP_000760.1:n.643-101_643-95delinsTTATTTA
NM_000769.4:c.643-101_643-95delinsTTATTTA MANE Select	NP_000760.1:n.643-101_643-95delinsTTATTTA