Canonical Allele Identifier: CA2629502923

Gene: CYP1A1

Linked Data

• gnomAD v4: 15-74719773-ACC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74719780_74719781del , CM000677.2:g.74719780_74719781del	GRCh38
NC_000015.9:g.75012121_75012122del , CM000677.1:g.75012121_75012122del	GRCh37
NC_000015.8:g.72799174_72799175del	NCBI36
NG_008431.1:g.2239_2240del
NG_008431.2:g.2239_2240del
NG_061374.1:g.10754_10755del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.*714_*715del MANE Select	ENSP00000369050.3:n.*714_*715del
ENST00000379727.7:c.*714_*715del	ENSP00000369050.3:n.*714_*715del
ENST00000395048.6:c.*714_*715del	ENSP00000378488.2:n.*714_*715del
ENST00000612821.4:c.2169_2170del	ENSP00000479744.1:n.2169_2170del
ENST00000617691.4:c.*714_*715del	ENSP00000482863.1:n.*714_*715del
NM_000499.3:c.*714_*715del	NP_000490.1:n.*714_*715del
XM_005254185.1:c.*714_*715del	XP_005254242.1:n.*714_*715del
NM_000499.5:c.*714_*715del	NP_000490.1:n.*714_*715del
NM_001319216.2:c.*714_*715del	NP_001306145.1:n.*714_*715del
NM_001319217.2:c.*714_*715del MANE Select	NP_001306146.1:n.*714_*715del