Canonical Allele Identifier: CA3893234

Gene: COL12A1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.75138491A>T , CM000668.2:g.75138491A>T	GRCh38
NC_000006.11:g.75848207A>T , CM000668.1:g.75848207A>T	GRCh37
NC_000006.10:g.75904927A>T	NCBI36
NG_042181.1:g.72417T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004370.6:c.5187T>A MANE Select	NP_004361.3:p.Pro1729=
ENST00000322507.13:c.5187T>A MANE Select	ENSP00000325146.8:p.Pro1729=
NM_004370.5:c.5187T>A	NP_004361.3:p.Pro1729=
NM_080645.2:c.1695T>A	NP_542376.2:p.Pro565=
NM_080645.3:c.1695T>A	NP_542376.2:p.Pro565=
ENST00000322507.12:c.5187T>A	ENSP00000325146.8:p.Pro1729=
ENST00000345356.10:c.1695T>A	ENSP00000305147.9:p.Pro565=
ENST00000416123.6:c.5187T>A	ENSP00000412864.2:p.Pro1729=
ENST00000419671.1:c.1411T>A
ENST00000483888.6:c.5187T>A	ENSP00000421216.1:p.Pro1729=
ENST00000615798.4:c.1620T>A	ENSP00000483232.1:p.Pro540=
XM_011535434.1:c.5187T>A	XP_011533736.1:p.Pro1729=
XM_011535435.1:c.4914T>A	XP_011533737.1:p.Pro1638=
XM_011535436.1:c.1695T>A	XP_011533738.1:p.Pro565=
XM_011535436.2:c.1695T>A	XP_011533738.1:p.Pro565=
XM_017010252.2:c.5151T>A	XP_016865741.1:p.Pro1717=