Canonical Allele Identifier: CA969760436

Gene: CYP19A1 PIRC66 MIR4713HG

Linked Data

• dbSNP Id: rs2033935403
• gnomAD v3: 15-51243994-CATACTCCAAGGTTTGCCTTTACTTAG-C
• gnomAD v4: 15-51243994-CATACTCCAAGGTTTGCCTTTACTTAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.51243996_51244021del , CM000677.2:g.51243996_51244021del	GRCh38
NC_000015.9:g.51536193_51536218del , CM000677.1:g.51536193_51536218del	GRCh37
NC_000015.8:g.49323485_49323510del	NCBI36
NG_007982.1:g.99579_99604del

Transcript Alleles

HGVS	Amino-acid change
ENST00000396402.6:c.-38-1070_-38-1045del (CYP19A1) MANE Select	ENSP00000379683.1:n.-38-1070_-38-1045del
ENST00000260433.6:c.-38-1070_-38-1045del (CYP19A1)	ENSP00000260433.2:n.-38-1070_-38-1045del
ENST00000396402.5:c.-38-1070_-38-1045del (CYP19A1)	ENSP00000379683.1:n.-38-1070_-38-1045del
ENST00000396404.8:c.-38-1070_-38-1045del (CYP19A1)	ENSP00000379685.4:n.-38-1070_-38-1045del
ENST00000405011.6:c.-38-1070_-38-1045del (CYP19A1)	ENSP00000384389.2:n.-38-1070_-38-1045del
ENST00000439712.6:c.-38-1070_-38-1045del (CYP19A1)	ENSP00000390614.2:n.-38-1070_-38-1045del
ENST00000453807.6:c.-38-1070_-38-1045del (CYP19A1)	ENSP00000391139.2:n.-38-1070_-38-1045del
ENST00000557858.5:c.-38-1070_-38-1045del (CYP19A1)	ENSP00000452627.1:n.-38-1070_-38-1045del
ENST00000557934.5:c.-38-1070_-38-1045del (CYP19A1)	ENSP00000454004.1:n.-38-1070_-38-1045del
ENST00000558328.5:c.-38-1070_-38-1045del (CYP19A1)	ENSP00000453280.1:n.-38-1070_-38-1045del
ENST00000559646.1:c.-38-1070_-38-1045del (CYP19A1)	ENSP00000453318.1:n.-38-1070_-38-1045del
ENST00000559980.5:c.-38-1070_-38-1045del (CYP19A1)	ENSP00000452872.1:n.-38-1070_-38-1045del
ENST00000561075.5:c.-38-1070_-38-1045del (CYP19A1)	ENSP00000454039.1:n.-38-1070_-38-1045del
NM_000103.3:c.-38-1070_-38-1045del (CYP19A1)	NP_000094.2:n.-38-1070_-38-1045del
NM_031226.2:c.-38-1070_-38-1045del (CYP19A1)	NP_112503.1:n.-38-1070_-38-1045del
XM_005254191.1:c.-38-1070_-38-1045del (CYP19A1)	XP_005254248.1:n.-38-1070_-38-1045del
XR_932222.1:n.99-33987_99-33962del (PIRC66)
NM_001347248.1:c.-38-1070_-38-1045del (CYP19A1)	NP_001334177.1:n.-38-1070_-38-1045del
NM_001347249.1:c.-38-1070_-38-1045del (CYP19A1)	NP_001334178.1:n.-38-1070_-38-1045del
NM_001347250.1:c.-38-1070_-38-1045del (CYP19A1)	NP_001334179.1:n.-38-1070_-38-1045del
NM_001347251.1:c.-38-1070_-38-1045del (CYP19A1)	NP_001334180.1:n.-38-1070_-38-1045del
NM_001347252.1:c.-38-1070_-38-1045del (CYP19A1)	NP_001334181.1:n.-38-1070_-38-1045del
NM_001347253.1:c.-38-1070_-38-1045del (CYP19A1)	NP_001334182.1:n.-38-1070_-38-1045del
NR_146310.1:n.195-33987_195-33962del (MIR4713HG)
NM_000103.4:c.-38-1070_-38-1045del (CYP19A1) MANE Select	NP_000094.2:n.-38-1070_-38-1045del
NM_001347249.2:c.-38-1070_-38-1045del (CYP19A1)	NP_001334178.1:n.-38-1070_-38-1045del
NM_031226.3:c.-38-1070_-38-1045del (CYP19A1)	NP_112503.1:n.-38-1070_-38-1045del
NM_001347250.2:c.-38-1070_-38-1045del (CYP19A1)	NP_001334179.1:n.-38-1070_-38-1045del
NM_001347251.2:c.-38-1070_-38-1045del (CYP19A1)	NP_001334180.1:n.-38-1070_-38-1045del
NM_001347252.2:c.-38-1070_-38-1045del (CYP19A1)	NP_001334181.1:n.-38-1070_-38-1045del
NM_001347253.2:c.-38-1070_-38-1045del (CYP19A1)	NP_001334182.1:n.-38-1070_-38-1045del