Canonical Allele Identifier: CA3893236

Gene: COL12A1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.75138498A>C , CM000668.2:g.75138498A>C	GRCh38
NC_000006.11:g.75848214A>C , CM000668.1:g.75848214A>C	GRCh37
NC_000006.10:g.75904934A>C	NCBI36
NG_042181.1:g.72410T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_004370.6:c.5180T>G MANE Select	NP_004361.3:p.Ile1727Ser
ENST00000322507.13:c.5180T>G MANE Select	ENSP00000325146.8:p.Ile1727Ser
NM_004370.5:c.5180T>G	NP_004361.3:p.Ile1727Ser
NM_080645.2:c.1688T>G	NP_542376.2:p.Ile563Ser
NM_080645.3:c.1688T>G	NP_542376.2:p.Ile563Ser
ENST00000322507.12:c.5180T>G	ENSP00000325146.8:p.Ile1727Ser
ENST00000345356.10:c.1688T>G	ENSP00000305147.9:p.Ile563Ser
ENST00000416123.6:c.5180T>G	ENSP00000412864.2:p.Ile1727Ser
ENST00000419671.1:c.1404T>G
ENST00000483888.6:c.5180T>G	ENSP00000421216.1:p.Ile1727Ser
ENST00000615798.4:c.1613T>G	ENSP00000483232.1:p.Ile538Ser
XM_011535434.1:c.5180T>G	XP_011533736.1:p.Ile1727Ser
XM_011535435.1:c.4907T>G	XP_011533737.1:p.Ile1636Ser
XM_011535436.1:c.1688T>G	XP_011533738.1:p.Ile563Ser
XM_011535436.2:c.1688T>G	XP_011533738.1:p.Ile563Ser
XM_017010252.2:c.5144T>G	XP_016865741.1:p.Ile1715Ser