Canonical Allele Identifier: CA1638950566

Gene: COL12A1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.75087586C= , CM000668.2:g.75087586C=	GRCh38
NC_000006.11:g.75797302C= , CM000668.1:g.75797302C=	GRCh37
NC_000006.10:g.75854022C=	NCBI36
NG_042181.1:g.123322G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322507.13:c.9172G= MANE Select	ENSP00000325146.8:p.Gly3058=
ENST00000680981.1:n.581G=
ENST00000681086.1:n.955G=
ENST00000322507.12:c.9172G=	ENSP00000325146.8:p.Gly3058=
ENST00000345356.10:c.5680G=	ENSP00000305147.9:p.Gly1894=
ENST00000416123.6:c.8944G=	ENSP00000412864.2:p.Gly2982=
ENST00000425443.6:c.2086G=	ENSP00000399812.2:p.Gly696=
ENST00000483888.6:c.9160G=	ENSP00000421216.1:p.Gly3054=
ENST00000615798.4:c.5605G=	ENSP00000483232.1:p.Gly1869=
NM_004370.5:c.9172G=	NP_004361.3:p.Gly3058=
NM_080645.2:c.5680G=	NP_542376.2:p.Gly1894=
XM_011535434.1:c.9172G=	XP_011533736.1:p.Gly3058=
XM_011535435.1:c.8899G=	XP_011533737.1:p.Gly2967=
XM_011535436.1:c.5680G=	XP_011533738.1:p.Gly1894=
XM_011535436.2:c.5680G=	XP_011533738.1:p.Gly1894=
XM_017010252.2:c.9136G=	XP_016865741.1:p.Gly3046=
NM_004370.6:c.9172G= MANE Select	NP_004361.3:p.Gly3058=
NM_080645.3:c.5680G=	NP_542376.2:p.Gly1894=