Canonical Allele Identifier: CA3893384

Gene: COL12A1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.75145337C>T , CM000668.2:g.75145337C>T	GRCh38
NC_000006.11:g.75855053C>T , CM000668.1:g.75855053C>T	GRCh37
NC_000006.10:g.75911773C>T	NCBI36
NG_042181.1:g.65571G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004370.6:c.4679G>A MANE Select	NP_004361.3:p.Arg1560Gln
ENST00000322507.13:c.4679G>A MANE Select	ENSP00000325146.8:p.Arg1560Gln
NM_004370.5:c.4679G>A	NP_004361.3:p.Arg1560Gln
NM_080645.2:c.1187G>A	NP_542376.2:p.Arg396Gln
NM_080645.3:c.1187G>A	NP_542376.2:p.Arg396Gln
ENST00000322507.12:c.4679G>A	ENSP00000325146.8:p.Arg1560Gln
ENST00000345356.10:c.1187G>A	ENSP00000305147.9:p.Arg396Gln
ENST00000416123.6:c.4679G>A	ENSP00000412864.2:p.Arg1560Gln
ENST00000419671.1:c.903G>A
ENST00000474564.1:n.303G>A
ENST00000483888.6:c.4679G>A	ENSP00000421216.1:p.Arg1560Gln
ENST00000615798.4:c.1112G>A	ENSP00000483232.1:p.Arg371Gln
XM_011535434.1:c.4679G>A	XP_011533736.1:p.Arg1560Gln
XM_011535435.1:c.4406G>A	XP_011533737.1:p.Arg1469Gln
XM_011535436.1:c.1187G>A	XP_011533738.1:p.Arg396Gln
XM_011535436.2:c.1187G>A	XP_011533738.1:p.Arg396Gln
XM_017010252.2:c.4643G>A	XP_016865741.1:p.Arg1548Gln