Canonical Allele Identifier: CA13189015

Gene: CXCL12

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.44384759C>G , CM000672.2:g.44384759C>G	GRCh38
NC_000010.10:g.44880207C>G , CM000672.1:g.44880207C>G	GRCh37
NC_000010.9:g.44200213C>G	NCBI36
NG_016861.1:g.5339G>C
NG_016861.2:g.5339G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_199168.4:c.61+186G>C MANE Select	NP_954637.1:n.61+186G>C
ENST00000343575.11:c.61+186G>C MANE Select	ENSP00000339913.6:n.61+186G>C
NM_000609.6:c.61+186G>C	NP_000600.1:n.61+186G>C
NM_000609.7:c.61+186G>C	NP_000600.1:n.61+186G>C
NM_001033886.2:c.61+186G>C	NP_001029058.1:n.61+186G>C
NM_001178134.1:c.61+186G>C	NP_001171605.1:n.61+186G>C
NM_001178134.2:c.61+186G>C	NP_001171605.1:n.61+186G>C
NM_001277990.1:c.61+186G>C	NP_001264919.1:n.61+186G>C
NM_001277990.2:c.61+186G>C	NP_001264919.1:n.61+186G>C
NM_199168.3:c.61+186G>C	NP_954637.1:n.61+186G>C
ENST00000343575.10:c.61+186G>C	ENSP00000339913.6:n.61+186G>C
ENST00000374426.6:c.61+186G>C	ENSP00000363548.2:n.61+186G>C
ENST00000374429.6:c.61+186G>C	ENSP00000363551.2:n.61+186G>C
ENST00000395793.7:c.61+186G>C	ENSP00000379139.3:n.61+186G>C
ENST00000395794.2:c.61+186G>C	ENSP00000379140.2:n.61+186G>C
ENST00000395795.5:c.61+186G>C	ENSP00000379141.5:n.61+186G>C
ENST00000488591.1:n.126+186G>C
ENST00000496375.1:n.518+1217G>C
XR_001747171.1:n.126+186G>C
XR_001747172.1:n.126+186G>C
XR_001747173.1:n.126+186G>C
XR_001747174.1:n.126+186G>C