Canonical Allele Identifier: CA3893448

Gene: COL12A1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.75146240T>C , CM000668.2:g.75146240T>C	GRCh38
NC_000006.11:g.75855956T>C , CM000668.1:g.75855956T>C	GRCh37
NC_000006.10:g.75912676T>C	NCBI36
NG_042181.1:g.64668A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_004370.6:c.4422A>G MANE Select	NP_004361.3:p.Pro1474=
ENST00000322507.13:c.4422A>G MANE Select	ENSP00000325146.8:p.Pro1474=
NM_004370.5:c.4422A>G	NP_004361.3:p.Pro1474=
NM_080645.2:c.930A>G	NP_542376.2:p.Pro310=
NM_080645.3:c.930A>G	NP_542376.2:p.Pro310=
ENST00000322507.12:c.4422A>G	ENSP00000325146.8:p.Pro1474=
ENST00000345356.10:c.930A>G	ENSP00000305147.9:p.Pro310=
ENST00000416123.6:c.4422A>G	ENSP00000412864.2:p.Pro1474=
ENST00000419671.1:c.646A>G
ENST00000474564.1:n.46A>G
ENST00000483888.6:c.4422A>G	ENSP00000421216.1:p.Pro1474=
ENST00000615798.4:c.855A>G	ENSP00000483232.1:p.Pro285=
XM_011535434.1:c.4422A>G	XP_011533736.1:p.Pro1474=
XM_011535435.1:c.4149A>G	XP_011533737.1:p.Pro1383=
XM_011535436.1:c.930A>G	XP_011533738.1:p.Pro310=
XM_011535436.2:c.930A>G	XP_011533738.1:p.Pro310=
XM_017010252.2:c.4386A>G	XP_016865741.1:p.Pro1462=