Canonical Allele Identifier: CA3892988
Community Standard Title: NM_004370.6(COL12A1):c.5840C>T (p.Pro1947Leu)
Gene: COL12A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.75132037G>A , CM000668.2:g.75132037G>A GRCh38
NC_000006.11:g.75841753G>A , CM000668.1:g.75841753G>A GRCh37
NC_000006.10:g.75898473G>A NCBI36
NG_042181.1:g.78871C>T

Transcript Alleles

HGVS Amino-acid Change
NM_004370.6:c.5840C>T MANE Select NP_004361.3:p.Pro1947Leu
ENST00000322507.13:c.5840C>T MANE Select ENSP00000325146.8:p.Pro1947Leu
NM_004370.5:c.5840C>T NP_004361.3:p.Pro1947Leu
NM_080645.2:c.2348C>T NP_542376.2:p.Pro783Leu
NM_080645.3:c.2348C>T NP_542376.2:p.Pro783Leu
ENST00000322507.12:c.5840C>T ENSP00000325146.8:p.Pro1947Leu
ENST00000345356.10:c.2348C>T ENSP00000305147.9:p.Pro783Leu
ENST00000416123.6:c.5840C>T ENSP00000412864.2:p.Pro1947Leu
ENST00000483888.6:c.5840C>T ENSP00000421216.1:p.Pro1947Leu
ENST00000615798.4:c.2273C>T ENSP00000483232.1:p.Pro758Leu
XM_011535434.1:c.5840C>T XP_011533736.1:p.Pro1947Leu
XM_011535435.1:c.5567C>T XP_011533737.1:p.Pro1856Leu
XM_011535436.1:c.2348C>T XP_011533738.1:p.Pro783Leu
XM_011535436.2:c.2348C>T XP_011533738.1:p.Pro783Leu
XM_017010252.2:c.5804C>T XP_016865741.1:p.Pro1935Leu