Canonical Allele Identifier: CA491488100

Gene: CYP1A1

Linked Data

• MyVariant Identifiers: chr15:g.75012938C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74720597C>G , CM000677.2:g.74720597C>G	GRCh38
NC_000015.9:g.75012938C>G , CM000677.1:g.75012938C>G	GRCh37
NC_000015.8:g.72799991C>G	NCBI36
NG_008431.1:g.3056C>G
NG_008431.2:g.3056C>G
NG_061374.1:g.9932G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.1431G>C MANE Select	ENSP00000369050.3:p.Arg477=
ENST00000379727.7:c.1431G>C	ENSP00000369050.3:p.Arg477=
ENST00000395048.6:c.1431G>C	ENSP00000378488.2:p.Arg477=
ENST00000395049.8:c.1344G>C	ENSP00000378489.4:p.Arg448=
ENST00000567032.5:c.1431G>C	ENSP00000456585.1:p.Arg477=
ENST00000612821.4:c.1347G>C	ENSP00000479744.1:p.Arg449=
ENST00000617691.4:c.1344G>C	ENSP00000482863.1:p.Arg448=
NM_000499.3:c.1431G>C	NP_000490.1:p.Arg477=
XM_005254185.1:c.1431G>C	XP_005254242.1:p.Arg477=
NM_000499.5:c.1431G>C	NP_000490.1:p.Arg477=
NM_001319216.2:c.1344G>C	NP_001306145.1:p.Arg448=
NM_001319217.2:c.1431G>C MANE Select	NP_001306146.1:p.Arg477=