Canonical Allele Identifier: CA168098031

Linked Data

dbSNP Id: rs906191454
MyVariant Identifiers: chr7:g.141927382T>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.141927382T>G , CM000669.2:g.141927382T>G GRCh38
NC_000007.13:g.141627182T>G , CM000669.1:g.141627182T>G GRCh37
NC_000007.12:g.141273651T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000546910.6:c.*2722A>C (CLEC5A) MANE Select ENSP00000449999.1:n.*2722A>C
ENST00000465654.5:c.-179-18439T>G (MGAM) ENSP00000419372.1:n.-179-18439T>G
ENST00000497554.1:n.37-2395T>G (MGAM)
ENST00000546910.5:c.*2722A>C (CLEC5A) ENSP00000449999.1:n.*2722A>C
NM_001301167.1:c.*2722A>C (CLEC5A) NP_001288096.1:n.*2722A>C
NM_013252.2:c.*2722A>C (CLEC5A) NP_037384.1:n.*2722A>C
XM_011515783.1:c.*24+7538T>G (OR9A4) XP_011514085.1:n.*24+7538T>G
XM_011515995.1:c.*2722A>C (CLEC5A) XP_011514297.1:n.*2722A>C
XR_927428.1:n.2673A>C (CLEC5A)
XM_011515995.2:c.*2722A>C (CLEC5A) XP_011514297.1:n.*2722A>C
XM_017011915.1:c.*2722A>C (CLEC5A) XP_016867404.1:n.*2722A>C
XM_017011917.1:c.*2790A>C (CLEC5A) XP_016867406.1:n.*2790A>C
NM_013252.3:c.*2722A>C (CLEC5A) MANE Select NP_037384.1:n.*2722A>C
NM_001301167.2:c.*2722A>C (CLEC5A) NP_001288096.1:n.*2722A>C