Canonical Allele Identifier: CA7950811

Gene: CRYM

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.21278054G>C , CM000678.2:g.21278054G>C	GRCh38
NC_000016.9:g.21289375G>C , CM000678.1:g.21289375G>C	GRCh37
NC_000016.8:g.21196876G>C	NCBI36
NG_011610.1:g.30043C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001376256.1:c.170+28C>G MANE Select	NP_001363185.1:n.170+28C>G
ENST00000572914.2:c.170+28C>G MANE Select	ENSP00000461904.2:n.170+28C>G
NM_001888.4:c.170+28C>G	NP_001879.1:n.170+28C>G
NM_001888.5:c.170+28C>G	NP_001879.1:n.170+28C>G
ENST00000219599.7:c.170+28C>G	ENSP00000219599.3:n.170+28C>G
ENST00000219599.8:c.170+28C>G	ENSP00000219599.3:n.170+28C>G
ENST00000543948.5:c.170+28C>G	ENSP00000440227.1:n.170+28C>G
ENST00000571666.1:n.164+28C>G
ENST00000572914.1:c.170+28C>G	ENSP00000461904.1:n.170+28C>G
ENST00000574448.5:c.170+28C>G	ENSP00000459982.1:n.170+28C>G
ENST00000576703.5:c.44+28C>G	ENSP00000460126.1:n.44+28C>G
XM_011545740.1:c.170+28C>G	XP_011544042.1:n.170+28C>G
XM_024450157.1:c.170+28C>G	XP_024305925.1:n.170+28C>G