Canonical Allele Identifier: CA3893038

Gene: COL12A1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.75133414G>C , CM000668.2:g.75133414G>C	GRCh38
NC_000006.11:g.75843130G>C , CM000668.1:g.75843130G>C	GRCh37
NC_000006.10:g.75899850G>C	NCBI36
NG_042181.1:g.77494C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_004370.6:c.5673C>G MANE Select	NP_004361.3:p.Ile1891Met
ENST00000322507.13:c.5673C>G MANE Select	ENSP00000325146.8:p.Ile1891Met
NM_004370.5:c.5673C>G	NP_004361.3:p.Ile1891Met
NM_080645.2:c.2181C>G	NP_542376.2:p.Ile727Met
NM_080645.3:c.2181C>G	NP_542376.2:p.Ile727Met
ENST00000322507.12:c.5673C>G	ENSP00000325146.8:p.Ile1891Met
ENST00000345356.10:c.2181C>G	ENSP00000305147.9:p.Ile727Met
ENST00000416123.6:c.5673C>G	ENSP00000412864.2:p.Ile1891Met
ENST00000419671.1:c.1876C>G
ENST00000483888.6:c.5673C>G	ENSP00000421216.1:p.Ile1891Met
ENST00000615798.4:c.2106C>G	ENSP00000483232.1:p.Ile702Met
XM_011535434.1:c.5673C>G	XP_011533736.1:p.Ile1891Met
XM_011535435.1:c.5400C>G	XP_011533737.1:p.Ile1800Met
XM_011535436.1:c.2181C>G	XP_011533738.1:p.Ile727Met
XM_011535436.2:c.2181C>G	XP_011533738.1:p.Ile727Met
XM_017010252.2:c.5637C>G	XP_016865741.1:p.Ile1879Met