Canonical Allele Identifier: CA3892302

Gene: COL12A1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.75102676C>T , CM000668.2:g.75102676C>T	GRCh38
NC_000006.11:g.75812392C>T , CM000668.1:g.75812392C>T	GRCh37
NC_000006.10:g.75869112C>T	NCBI36
NG_042181.1:g.108232G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004370.6:c.8336G>A MANE Select	NP_004361.3:p.Arg2779His
ENST00000322507.13:c.8336G>A MANE Select	ENSP00000325146.8:p.Arg2779His
NM_004370.5:c.8336G>A	NP_004361.3:p.Arg2779His
NM_080645.2:c.4844G>A	NP_542376.2:p.Arg1615His
NM_080645.3:c.4844G>A	NP_542376.2:p.Arg1615His
ENST00000322507.12:c.8336G>A	ENSP00000325146.8:p.Arg2779His
ENST00000345356.10:c.4844G>A	ENSP00000305147.9:p.Arg1615His
ENST00000416123.6:c.8108G>A	ENSP00000412864.2:p.Arg2703His
ENST00000425443.6:c.1250G>A	ENSP00000399812.2:p.Arg417His
ENST00000483888.6:c.8336G>A	ENSP00000421216.1:p.Arg2779His
ENST00000615798.4:c.4769G>A	ENSP00000483232.1:p.Arg1590His
XM_011535434.1:c.8336G>A	XP_011533736.1:p.Arg2779His
XM_011535435.1:c.8063G>A	XP_011533737.1:p.Arg2688His
XM_011535436.1:c.4844G>A	XP_011533738.1:p.Arg1615His
XM_011535436.2:c.4844G>A	XP_011533738.1:p.Arg1615His
XM_017010252.2:c.8300G>A	XP_016865741.1:p.Arg2767His