Canonical Allele Identifier: CA3894538

Gene: COL12A1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.75202774G>C , CM000668.2:g.75202774G>C	GRCh38
NC_000006.11:g.75912490G>C , CM000668.1:g.75912490G>C	GRCh37
NC_000006.10:g.75969210G>C	NCBI36
NG_042181.1:g.8134C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_004370.6:c.19C>G MANE Select	NP_004361.3:p.Pro7Ala
ENST00000322507.13:c.19C>G MANE Select	ENSP00000325146.8:p.Pro7Ala
NM_004370.5:c.19C>G	NP_004361.3:p.Pro7Ala
NM_080645.2:c.19C>G	NP_542376.2:p.Pro7Ala
NM_080645.3:c.19C>G	NP_542376.2:p.Pro7Ala
ENST00000322507.12:c.19C>G	ENSP00000325146.8:p.Pro7Ala
ENST00000345356.10:c.19C>G	ENSP00000305147.9:p.Pro7Ala
ENST00000416123.6:c.19C>G	ENSP00000412864.2:p.Pro7Ala
ENST00000483888.6:c.19C>G	ENSP00000421216.1:p.Pro7Ala
ENST00000615798.4:c.-3549C>G	ENSP00000483232.1:n.-3549C>G
ENST00000680102.1:n.545C>G
XM_011535434.1:c.19C>G	XP_011533736.1:p.Pro7Ala
XM_011535435.1:c.19C>G	XP_011533737.1:p.Pro7Ala
XM_011535436.1:c.19C>G	XP_011533738.1:p.Pro7Ala
XM_011535436.2:c.19C>G	XP_011533738.1:p.Pro7Ala