Canonical Allele Identifier: CA491488335

Gene: CYP1A1

Linked Data

• MyVariant Identifiers: chr15:g.75013061A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74720720A>G , CM000677.2:g.74720720A>G	GRCh38
NC_000015.9:g.75013061A>G , CM000677.1:g.75013061A>G	GRCh37
NC_000015.8:g.72800114A>G	NCBI36
NG_008431.1:g.3179A>G
NG_008431.2:g.3179A>G
NG_061374.1:g.9809T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.1308T>C MANE Select	ENSP00000369050.3:p.Asp436=
ENST00000379727.7:c.1308T>C	ENSP00000369050.3:p.Asp436=
ENST00000395048.6:c.1308T>C	ENSP00000378488.2:p.Asp436=
ENST00000395049.8:c.1221T>C	ENSP00000378489.4:p.Asp407=
ENST00000562201.5:c.*545T>C	ENSP00000455340.1:n.*545T>C
ENST00000564596.5:c.*243T>C	ENSP00000457668.1:n.*243T>C
ENST00000566503.1:c.525T>C	ENSP00000455846.1:p.Asp175=
ENST00000567032.5:c.1308T>C	ENSP00000456585.1:p.Asp436=
ENST00000569630.5:c.*897T>C	ENSP00000455051.1:n.*897T>C
ENST00000612821.4:c.1224T>C	ENSP00000479744.1:p.Asp408=
ENST00000617691.4:c.1221T>C	ENSP00000482863.1:p.Asp407=
NM_000499.3:c.1308T>C	NP_000490.1:p.Asp436=
XM_005254185.1:c.1308T>C	XP_005254242.1:p.Asp436=
NM_000499.5:c.1308T>C	NP_000490.1:p.Asp436=
NM_001319216.2:c.1221T>C	NP_001306145.1:p.Asp407=
NM_001319217.2:c.1308T>C MANE Select	NP_001306146.1:p.Asp436=