Canonical Allele Identifier: CA1573530022

Gene: SRP19

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112861940T>C , CM000667.2:g.112861940T>C	GRCh38
NC_000005.9:g.112197637T>C , CM000667.1:g.112197637T>C	GRCh37
NC_000005.8:g.112225536T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_003135.3:c.41+523T>C MANE Select	NP_003126.1:n.41+523T>C
ENST00000505459.6:c.41+523T>C MANE Select	ENSP00000424870.1:n.41+523T>C
NM_001204193.1:c.41+523T>C	NP_001191122.1:n.41+523T>C
NM_001204193.2:c.41+523T>C	NP_001191122.1:n.41+523T>C
NM_001204194.1:c.41+523T>C	NP_001191123.1:n.41+523T>C
NM_001204194.2:c.41+523T>C	NP_001191123.1:n.41+523T>C
NM_001204196.1:c.41+523T>C	NP_001191125.1:n.41+523T>C
NM_001204196.2:c.41+523T>C	NP_001191125.1:n.41+523T>C
NM_001204199.1:c.41+523T>C	NP_001191128.1:n.41+523T>C
NM_001204199.2:c.41+523T>C	NP_001191128.1:n.41+523T>C
NM_003135.2:c.41+523T>C	NP_003126.1:n.41+523T>C
ENST00000282999.7:c.41+523T>C	ENSP00000282999.3:n.41+523T>C
ENST00000391338.3:c.41+523T>C	ENSP00000375133.2:n.41+523T>C
ENST00000445150.3:c.41+523T>C	ENSP00000480521.1:n.41+523T>C
ENST00000503445.5:n.230+523T>C
ENST00000505459.5:c.41+523T>C	ENSP00000424870.1:n.41+523T>C
ENST00000506997.1:c.41+523T>C	ENSP00000424153.1:n.41+523T>C
ENST00000506997.2:c.41+523T>C	ENSP00000424153.1:n.41+523T>C
ENST00000512790.5:n.113+523T>C
ENST00000515463.1:c.41+523T>C	ENSP00000425562.1:n.41+523T>C
ENST00000515755.1:n.92+523T>C
ENST00000520401.1:c.256-568T>C
ENST00000621420.5:c.41+523T>C	ENSP00000482018.1:n.41+523T>C