Canonical Allele Identifier: CA3894500

Gene: COL12A1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.75194848G>A , CM000668.2:g.75194848G>A	GRCh38
NC_000006.11:g.75904564G>A , CM000668.1:g.75904564G>A	GRCh37
NC_000006.10:g.75961284G>A	NCBI36
NG_042181.1:g.16060C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004370.6:c.173C>T MANE Select	NP_004361.3:p.Thr58Met
ENST00000322507.13:c.173C>T MANE Select	ENSP00000325146.8:p.Thr58Met
NM_004370.5:c.173C>T	NP_004361.3:p.Thr58Met
NM_080645.2:c.73+7872C>T	NP_542376.2:n.73+7872C>T
NM_080645.3:c.73+7872C>T	NP_542376.2:n.73+7872C>T
ENST00000322507.12:c.173C>T	ENSP00000325146.8:p.Thr58Met
ENST00000345356.10:c.73+7872C>T	ENSP00000305147.9:n.73+7872C>T
ENST00000416123.6:c.173C>T	ENSP00000412864.2:p.Thr58Met
ENST00000483888.6:c.173C>T	ENSP00000421216.1:p.Thr58Met
ENST00000615798.4:c.-3395C>T	ENSP00000483232.1:n.-3395C>T
XM_011535434.1:c.173C>T	XP_011533736.1:p.Thr58Met
XM_011535435.1:c.173C>T	XP_011533737.1:p.Thr58Met
XM_011535436.1:c.73+7872C>T	XP_011533738.1:n.73+7872C>T
XM_011535436.2:c.73+7872C>T	XP_011533738.1:n.73+7872C>T
XM_017010252.2:c.137C>T	XP_016865741.1:p.Thr46Met