Canonical Allele Identifier: CA3893239

Gene: COL12A1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.75138538G>C , CM000668.2:g.75138538G>C	GRCh38
NC_000006.11:g.75848254G>C , CM000668.1:g.75848254G>C	GRCh37
NC_000006.10:g.75904974G>C	NCBI36
NG_042181.1:g.72370C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_004370.6:c.5140C>G MANE Select	NP_004361.3:p.Leu1714Val
ENST00000322507.13:c.5140C>G MANE Select	ENSP00000325146.8:p.Leu1714Val
NM_004370.5:c.5140C>G	NP_004361.3:p.Leu1714Val
NM_080645.2:c.1648C>G	NP_542376.2:p.Leu550Val
NM_080645.3:c.1648C>G	NP_542376.2:p.Leu550Val
ENST00000322507.12:c.5140C>G	ENSP00000325146.8:p.Leu1714Val
ENST00000345356.10:c.1648C>G	ENSP00000305147.9:p.Leu550Val
ENST00000416123.6:c.5140C>G	ENSP00000412864.2:p.Leu1714Val
ENST00000419671.1:c.1364C>G
ENST00000483888.6:c.5140C>G	ENSP00000421216.1:p.Leu1714Val
ENST00000615798.4:c.1573C>G	ENSP00000483232.1:p.Leu525Val
XM_011535434.1:c.5140C>G	XP_011533736.1:p.Leu1714Val
XM_011535435.1:c.4867C>G	XP_011533737.1:p.Leu1623Val
XM_011535436.1:c.1648C>G	XP_011533738.1:p.Leu550Val
XM_011535436.2:c.1648C>G	XP_011533738.1:p.Leu550Val
XM_017010252.2:c.5104C>G	XP_016865741.1:p.Leu1702Val